Defluorodearomatization: A Photocatalytic Birch-Like Reduction That Enables C–C Bond Formation and Provides Access to Unnatural Cannabinoids-Reference-Cited by-同舟云学术

Defluorodearomatization: A Photocatalytic Birch-Like Reduction That Enables C–C Bond Formation and Provides Access to Unnatural Cannabinoids

Published:2021-06-02 Issue:12 Volume:86 Page:7928-7945
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Day Jon I.¹^ORCID,Grotjahn Sascha²,Senaweera Sameera³,Koenig Burkhard²^ORCID,Weaver III Jimmie D.¹^ORCID

Affiliation:

1. Department of Chemistry, Oklahoma State University, 107 Physical Science, 74078 Stillwater, Oklahoma, United States

2. Institut für Organische Chemie, Universität Regensburg, Universitätstrasse 31, 93053 Regensburg, Germany

3. Center for Drug Design, College of Pharmacy, University of Minnesota, 7-158 Phillips Wangensteen Building, 516 Delaware Street SE, Minneapolis, Minnesota 55455, United States

Funder

Elitenetzwerk Bayern

Deutsche Forschungsgemeinschaft

National Institute of General Medical Sciences

H2020 European Research Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c00169

Reference81 articles.

1. Natural Occurrence of Organofluorine and Other Constituents from Streptomyces sp. TC1

2. Structure of a Putative Fluorinated Natural Product from Streptomyces sp. TC1

3. Total Synthesis of a Reported Fluorometabolite from Streptomyces sp. TC1 Indicates an Incorrect Assignment. The Isolated Compound Did Not Contain Fluorine

4. Correction to Natural Occurrence of Organofluorine and Other Constituents from Streptomyces sp. TC1

5. Fluorinated natural products: the biosynthesis of fluoroacetate and 4-fluorothreonine in Streptomyces cattleya

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