Stereocontrolled Synthesis Of The Corey Prostaglandin Intermediate, 7-Syn-Methoxymethyl-Bicyclo[2.2.1]Hept-5-En-2-One

Garry N. Fickes, Richard S. Glass

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

The key steps in the reported stereocontrolled synthesis of hicyclic ketone 2 are Diels-Alder reaction of 5-methoxymethyl-l,2,3,4,5-pentachloro-l,3-cyclopentadiene, 3, and vinyl acetate and stereocontrolled reductive dechlorination of bicyclic THP ether 4c.

Original languageEnglish (US)
Pages (from-to)721-728
Number of pages8
JournalSynthetic Communications
Volume13
Issue number9
DOIs
StatePublished - Jul 1 1983

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Stereocontrolled Synthesis Of The Corey Prostaglandin Intermediate, 7-Syn-Methoxymethyl-Bicyclo[2.2.1]Hept-5-En-2-One'. Together they form a unique fingerprint.

Cite this