A free radical route to syn lactones and other prostanoid intermediates in isoprostaglandin synthesis.-Reference-Cited by-同舟云学术

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A free radical route to syn lactones and other prostanoid intermediates in isoprostaglandin synthesis.

Published:1993-12 Issue:51 Volume:34 Page:8245-8248
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Rondot Benoît,Durand Thierry,Girard Jean Pierre,Rossi Jean Claude,Schio Laurent,Khanapure Subhash P.,Rokach Joshua

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. A series of prostaglandin F2-like compounds are produced in vivo in humans by a non-cyclooxygenase, free radical-catalyzed mechanism.

2. Preferential formation of 8-epi-prostaglandin f2α via the corresponding endoperoxide by a biomimetic cyclization

3. Efficient free-radical and palladium-catalyzed tandem alkene insertions: a new approach to benzoprostacyclins

4. Preferential cis cyclization of 6-hepten-2-yl and related radicals. Example of orbital symmetry control

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2. Isoprostanoids, Isofuranoids and Isoketals – From Synthesis to Lipidomics;European Journal of Organic Chemistry;2022-02-03

3. Stereoselective preparation of key intermediates for the synthesis of iso-, neuro- and phyto-prostane family members: inaugural asymmetric synthesis of 17-E2c-dihomo- and 17-F2c-dihomo-isoprostanes;Organic & Biomolecular Chemistry;2018

4. Isoprostanes, neuroprostanes and phytoprostanes: An overview of 25 years of research in chemistry and biology;Progress in Lipid Research;2017-10

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