Synthesis of Active Antifeedant CDE Fragments of 11-Ketoepoxyazadiradione Based on an Electrocyclization Reaction Catalyzed by Perchloric Acid-Reference-Cited by-同舟云学术

Synthesis of Active Antifeedant CDE Fragments of 11-Ketoepoxyazadiradione Based on an Electrocyclization Reaction Catalyzed by Perchloric Acid

Published:1998-11-20 Issue:25 Volume:63 Page:9440-9447
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Fernández-Mateos Alfonso¹,Martín de la Nava Eva M.¹,Pascual Coca Gustavo¹,Rubio González Rosa¹,Ramos Silvo Ana I.¹,Simmonds M. S. J.¹,Blaney W. M.¹

Affiliation:

1. Facultad de C. Químicas, Departamento de Química Orgánica, Universidad de Salamanca, Plaza de los Caídos 1−5, 37008 Salamanca, Spain, Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, U.K., and Department of Biology, Birkbeck College, Malet Street, London, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo981456q

Reference16 articles.

1. Stereoselective addition of enol silanes to nitro olefins. A simple synthesis of compounds related to the insect antifeedants azadiradione and gedunin

2. A novel non nucleoside compound with high in vitro anti-HIV-1 activity. Absolute stereochemistry determination

3. Biological activity of limonoids from the rutales

4. Limonoid Model Insect Antifeedants. A Stereoselective Synthesis of Azadiradione C, D, and E Fragments through Intramolecular Diazo Ketone Cyclization

5. Model insect antifeedants. Synthesis of azadiradione fragments through acyl radicals cyclizations and stannane coupling reactions

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