Enantioselective Total Synthesis of Eicosanoid and Its Congener, Using Organocatalytic Cyclopropanation, and Catalytic Asymmetric Transfer Hydrogenation Reactions as Key Steps-Reference-Cited by-同舟云学术

Enantioselective Total Synthesis of Eicosanoid and Its Congener, Using Organocatalytic Cyclopropanation, and Catalytic Asymmetric Transfer Hydrogenation Reactions as Key Steps

Published:2008-06-05 Issue:13 Volume:73 Page:5198-5201
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kumaraswamy Gullapalli¹,Padmaja Mogilisetti¹

Affiliation:

1. Organic Division III, Fine Chemicals Laboratory, Indian Institute of Chemical Technology, Hyderabad-500 607, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800631z

Reference46 articles.

1. Carbocyclic oxylipins of marine origin

2. Formation of a cyclopropyl eicosanoid via an allene oxide in the coral Plexaura homomalla: implications for the biosynthesis of 5,6-trans-prostaglandin A2

3. Halicholactone and neohalicholactone, two novel fatty acid metabolites from the marine sponge kadota

4. The three-dimensional structure of neohalicholactone, an unusual fatty acid metabolite from the marine sponge halichondria okadai kadota

5. Solandelactones A-I, lactonized cyclopropyl oxylipins isolated from the hydroid Solanderia secunda

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