Publications

2006

OKOTH, PROFOGENDOHASTINGW.  2006.  "Land policies in Sub-Saharan Africa: An Overview" in Akinyi Nzioki, Land Policies in Sub-Sahara Africa, Centre for Land,Economy and rights of women,. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2006.  "Land and Human Rights" paper submitted to the Kenya National Human Rights Commission for the 5th Edition of NGUZO ZA HAKI. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2006.  "Reforming Land Rights Administration Systems in Africa: A preliminary presentation of issues paper for the World bank Institute/UN-Habitat/University of Nairobi regional training course on land administration,May 22-25. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2006.  "Land Rights in Africa: Interrogating the tenure security discourse" paper for the IFAD MLWE UNOPS workshop on land tenure security.Kampla Uganda, June 26-30. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

2005

OKOTH, PROFOGENDOHASTINGW.  2005.  "Access to land in Africa: a fundamental human right", paper for the 14th Commonwealth Law Conference held in London, United Kingdom, September 11 - 15.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2005.  "Tenure issues in drylands development: tenue of land or tenure of ecological resources? Paper for the UNDP working on Drylands development, Nairobi, February 28- 2 March Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2005.  "Overview of legal, regulatory and institutional reforms in agriculture: the global perspective,paper for the national conference on the revitalising of the agricutural sector February 20-24.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

2004

OKOTH, PROFOGENDOHASTINGW.  2004.  "Integrating Climate Change Considerations in National Development Policies and Programes paper for a Workshop on dialohue with East African legislators on Climate Change and sustainable development, Safari Park hotel, nairobi, april 23-24.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2004.  "Climate Change Adaptation and Mitigation: Exploring the Role of Land Reforms in Africa" paper for the second colloquium of the IUCN Academy of International Law, held in Nairobi, Kenya, 4-7 October.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2004.  "Education in a globalising world"Paper for the First International Conference on the Right to Education organised by the European Association for Education Law and Policy in Amsterdam, the Netherlands, 26-30, November.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

2003

OKOTH, PROFOGENDOHASTINGW.  2003.  "The Role of Members of Parliament in law-making and representation" paper for the post-election seminar for Members of Parliament, Safari Park Hotel, Nairobi July 25-26.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2003.  "The legal Framework for Education in Kenya" paper for the National Conference on Education and Training in Kenya, Nairobi, November 26-28.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2003.  "Re-engineering land administration in Kenya: the case for a National Land Commission, Technical Paper for the Kenya Land Alliance. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

2002

OKOTH, PROFOGENDOHASTINGW.  2002.  "Land Administration: the Neglected factor in land reform in Africa", paper for the world Bank Regional Workshop on Land issues in Africa and the Middle East, held in Kampala, Uganda, april 29 - May 2.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2002.  "Land Tenure Reform in Africa: Lessons from East Africa", paper for the symposium on communal Land Tenure Reform, held in Johannesburg, south Africa, August 12-13.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  2002.  "The Tragic African Commons: A century of expropriation, suppression, and subversion, in Amplifying Local Voices: Striving for Environmental Justice, Centre for International Environmental Law, et. al. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

2001

OKOTH, PROFOGENDOHASTINGW.  2001.  "Land Rights, Food Security and Poverty", paper for the conference on Women and Land Rights in Eastern Africa held in Kampla, Uganda, October 28-November 1.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

2000

OKOTH, PROFOGENDOHASTINGW.  2000.  "Through the Interstices of Procedure: Creating democratic space for environmental management, paper for the East African Regional Workshop on environmental procedural rights, held in Entebbe, Uganda, November 23-24. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

1999

OKOTH, PROFOGENDOHASTINGW.  1999.  "The juridical framework of environmental governance" Chapter 3 in Governing the Environment (op. cit).. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1999.  "Land policy development in East Africa: a survey of recent trendes"; paper for DFID workshop on Land Rights and Sub-Saharan Africa Sunningdale, England, February 16-19.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1999.  "The Quest for Constitutional Government in Africa", Chapter 2, in African Perspectives on Governance (op.cit). Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1999.  "Present Concerns and Future Challenges in Land Policy Development in Africa", discussion issues at the Architectural Association of Kenya Conference for the Building Industry, Safari Park Hotel, Nairoi, May 19-21.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

1998

OKOTH, PROFOGENDOHASTINGW.  1998.  "Tenure regimes and land use systems in Africa: the challenge of sustainability"; in Towards Sustainable Land Use: Furthering cooperation between people and institutions. Edited by Blume. H.P. Eger et. Al Advances in GEO Ecology 3 (Catena Verglag AMBH).. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1998.  "Implementing Land Legislation in Uganda: Drawing on comparative experiences; paper for a technical workshop on the Uganda Land Act.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1998.  "Governance Beyond Government"; A rejoinder to Justice Breyer of the United states supreme Court and Prof. Frank Michelman of Harvard University Law School at a symposium organised by the US Association of Constitutional Law on constitutionalism Privatisa. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1998.  "Legislating land rights for the poor. A preliminary assessment of Uganda's Land Act 1998, paper for the Uganda Land Alliance Strategic Planning Workshop Mukono 6-8, September.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

1997

OKOTH, PROFOGENDOHASTINGW.  1997.  "Be fruitful and multiply: - population management in Africa on the eve of the 21st centry?: Population management in Africa into thenext millennium" Faculty Luncheon presentation, NewYork University School of Law. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

1996

OKOTH, PROFOGENDOHASTINGW.  1996.  "Global climate change and environmental governance: setting an African Agenda for policy responses on the United Nations Framework Convention on Climate Change, 1992", A concept Paper for the SEI/ACTS Climate and African Project. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1996.  "Land tenure and resource management: a comment:" in ENTWICKLUNG LANDLICHER RAUM Vol. 3 No. 2 Bonn, Germany. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1996.  "Land tenure and land administration in Tanzania: a paper for a Workshop on Land Use Planning and Land Tenure System", Sokoine University of agriculture, Morogoro, Tanzania, February.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1996.  "Land tenure and natural resource management: the Kenya experience", paper for the OSS/IGADD/ECA Workshop on Land tenure, Addis Ababa Ethiopia, March.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1996.  "Constitutionalism without Constitutions: the challenge of reconstruction of the state in Africa; in Zoethout C.M. etal Constitutionalism in Africa: A quest for Authoctonous Principles. Sanders Institute, Netherlands, March.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1996.  "Reforming land tenure in Africa: conceptual methodological and policy issues"; paper for the Alistair Berkeley Seminar on Land Tenure and Tenurial Reform London School of Economics and Political Science London May.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

1994

OKOTH, PROFOGENDOHASTINGW.  1994.  "Land tenure, agrarian legislation and environmental management systems"; in Bakama, R. J. (Ed.) Land Tenure and Sustainable Land Use (Chapter 2) KIT Bulletin 221, The Netherlands. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1994.  Population as a development issue: experiences from Kenya (Paper for an International Workshop on "Population Policy, Practices, Criticism and the View of Regions", Bonn, Germany, June 17-18.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

1993

OKOTH, PROFOGENDOHASTINGW.  1993.  "Human and People's Rights: What Point is Africa Trying to Make? In Ronald Cohen, Goran Hyden and Winston Nagan Human Rights and Governance in Africa (Chapter 3), University Press of Florida Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1993.  "Population growth and agricultural change in Kisii Dirctrict, Kenya: sustained symbiosis? (with John O. Oucho) (Chapter 6) in B. L. Turner II, Goran Hyden and Robert Kates, Population growth and Agricultural Change in Africa, University Press of Florida Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1993.  "Constitutions without constitutionalism: an African political paradox" in douglas Greenberg S.N. Kartz, B. Oliviero and S.C. Wheatley (Eds) Constitutionalism and Democracy: Transitions in the Contemporary World (Chapter 4) OUP, New York. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1993.  "Agrarian reform in Sub-Saharan Africa: assessment of state responses to the African Agrarian crisis and their implications for Agricultural Development". In Thomas J. Basset and CrummeyD.E. Land in African Agrarian Systems (Chapter 9) University of Wisco. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.
OKOTH, PROFOGENDOHASTINGW.  1993.  "Population and natural resources use"; a paper for the Population Summit of the world Academies of Sciencies held in New Delhi, India, October 24.. Cent. Afri. J. Pharm.Sci. 5(3): 60-66. : Cent. Afri. J. Pharm.Sci. 5(3): 60-66 Abstract
The identification of five novel compounds, pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-erythromycin A-6,9-hemiketal, 8,9-anhydro-pseudo-N-demethylerythromycin A-6,9-hemiketal, 5-O-beta-D-desosaminylerythronolide A and 15-nor-erythromycin C, in mother liquor concentrates of Streptomyces erythraeus is described. The pseudo-erythromycin derivatives are characterized by a 12-membered macrocyclic ring as a result of C13––C11 trans-lactonization. The five compounds have very little antimicrobial activity.

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