Campus Units

Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

5-1992

Journal or Book Title

The Journal of Organic Chemistry

Volume

57

Issue

10

First Page

2922

Last Page

2925

DOI

10.1021/jo00036a030

Abstract

The key step in a synthesis of 1 was a tandem photoenolization/Diels-Alder reaction to produce 11. Hydrolysis of the acetal and ester followed by oxidation afforded 15, an advanced intermediate in the Meyers synthesis of 1.

Comments

Reprinted (adapted) with permission from The Journal of Organic Chemistry, 57(10); 2922-2925. Doi: 10.1021/jo00036a030. Copyright 1992 American Chemical Society.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

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