Campus Units

Chemistry, Ames Laboratory

Document Type

Article

Publication Version

Published Version

Publication Date

4-28-2020

Journal or Book Title

ACS Omega

Volume

5

Issue

16

First Page

9311

Last Page

9315

DOI

10.1021/acsomega.0c00201

Abstract

A variety of nucleophiles react efficiently with in situ generated nitroquinones. The reaction with substituted resorcinols led to the direct synthesis of the phenanthroviridinone and lagumycin skeleton via a highly regioselective Diels–Alder reaction.

Comments

This article is published as Yu, Huangchao, Ellie L. Fought, Theresa L. Windus, and George A. Kraus. "Direct Synthesis of the Phenanthroviridone Skeleton Using a Highly Regioselective Nitroquinone Diels–Alder Reaction." ACS Omega 5, no. 16 (2020): 9311-9315. DOI: 10.1021/acsomega.0c00201. Posted with permission.

Rights

This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

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