Article
Direct Synthesis of the Phenanthroviridone Skeleton Using a Highly Regioselective Nitroquinone Diels–Alder Reaction
ACS Omega
Document Type
Article
Disciplines
Publication Version
Published Version
Publication Date
4-28-2020
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.
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
Copyright Date
2020
Language
en
File Format
application/pdf
Citation Information
Huangchao Yu, Ellie Fought, Theresa L. Windus and George A. Kraus. "Direct Synthesis of the Phenanthroviridone Skeleton Using a Highly Regioselective Nitroquinone Diels–Alder Reaction" ACS Omega Vol. 5 Iss. 16 (2020) p. 9311 - 9315 Available at: http://works.bepress.com/george_kraus/259/
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.