Total Synthesis of (15R)- and (15S)-F2t-Isoprostanes by a Biomimetic Process Using the Cyclization of Acyclic Dihydroxylated Octa-5,7-dienyl Radicals-Reference-Cited by-同舟云学术

Total Synthesis of (15R)- and (15S)-F2t-Isoprostanes by a Biomimetic Process Using the Cyclization of Acyclic Dihydroxylated Octa-5,7-dienyl Radicals

Published:2002-05-01 Issue:11 Volume:67 Page:3615-3624
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Durand Thierry¹,Guy Alexandre¹,Vidal Jean-Pierre¹,Rossi Jean-Claude¹

Affiliation:

1. Laboratoire de Chimie Biomoléculaire et Interactions Biologiques, associée au CNRS (UMR 5074), and Université Montpellier I, Faculté de Pharmacie, 15 Av. Charles Flahault, B.P. 14 491, F-34093 Montpellier Cedex 5, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0109624

Reference100 articles.

1. Prostaglandin Syntheses by Three-Component Coupling. New Synthetic Methods(49)

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4. New reagents for stereoselective carbonyl reduction. Improved synthetic route to the primary prostaglandins

5. Preparation of an optically active prostaglandin intermediate via asymmetric induction

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