Synthesis of the Azaphilones (+)-Sclerotiorin and (+)-8-O-Methylsclerotiorinamine Utilizing (+)-Sparteine Surrogates in Copper-Mediated Oxidative Dearomatization-Reference-Cited by-同舟云学术

Synthesis of the Azaphilones (+)-Sclerotiorin and (+)-8-O-Methylsclerotiorinamine Utilizing (+)-Sparteine Surrogates in Copper-Mediated Oxidative Dearomatization

Published:2011-03-14 Issue:8 Volume:76 Page:2577-2584
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Germain Andrew R.¹,Bruggemeyer Daniel M.¹,Zhu Jianglong¹,Genet Cedric²,O’Brien Peter²,Porco John A.¹

Affiliation:

1. Department of Chemistry, Center for Chemical Methodology and Library Development (CMLD-BU), Boston University, 590 Commonwealth Avenue, Boston, Massachusetts 02215, United States

2. Department of Chemistry, University of York, Heslington, York YO105DD, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo102448n

Reference40 articles.

1. Azaphilones: a class of fungal metabolites with diverse biological activities

2. Synthesis of the Azaphilones Using Copper-Mediated Enantioselective Oxidative Dearomatization

3. Enantioselective Synthesis of Bicyclo[2.2.2]octenones Using a Copper-Mediated Oxidative Dearomatization/[4 + 2] Dimerization Cascade

4. Tetrahedral Distortion in Copper(II) Complexes of (−)-Sparteine and Its Effect on the Oxygen Adduct Formation

5. Sclerotiorine, a Chlorinated Metabolic Product of Penicillium Sclerotiorum, Van Beyma

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