Campus Units

Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

4-1987

Journal or Book Title

The Journal of Organic Chemistry

Volume

52

Issue

7

First Page

1273

Last Page

1276

DOI

10.1021/jo00383a018

Abstract

Deoxyfrenolicin and nanaomycin A have been synthesized. Key steps in the synthesis include a phthalide annulation reaction to produce a naphthoquinone, a tandem Diels-Alder/retro-Claisen reaction to produce the carbon skeleton, and a stereoselective reduction of a hemiketal.

Comments

Reprinted (adapted) with permission from The Journal of Organic Chemistry, 52(7); 1273-1276. Doi: 10.1021/jo00383a018. Copyright 1987 American Chemical Society.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

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