Synthesis of Benzannulated Medium-ring Lactams via a Tandem Oxidative Dearomatization-Ring Expansion Reaction-Reference-Cited by-同舟云学术

Synthesis of Benzannulated Medium-ring Lactams via a Tandem Oxidative Dearomatization-Ring Expansion Reaction

Published:2018-08-02 Issue:50 Volume:24 Page:13150-13157
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Guney Tezcan¹,Wenderski Todd A.¹,Boudreau Matthew W.²,Tan Derek S.¹³^ORCID

Affiliation:

1. Chemical Biology Program, Sloan Kettering Institute; Memorial Sloan Kettering Cancer Center; 1275 York Avenue, Box 422 New York NY 10065 USA

2. Gerstner Sloan Kettering Summer Undergraduate Research Program; Memorial Sloan Kettering Cancer Center; 1275 York Avenue, Box 422 New York NY 10065 USA

3. Tri-Institutional Research Program; Memorial Sloan Kettering Cancer Center; 1275 York Avenue, Box 422 New York NY 10065 USA

Funder

National Institute of General Medical Sciences

National Cancer Institute

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201802880/fullpdf

Reference106 articles.

1. Importance and synthesis of benzannulated medium-sized and macrocyclic rings (BMRs)

2. Towards Diversity-Oriented, Stereoselective Syntheses of Biaryl- or Bis(aryl)metal-Containing Medium Rings

3. Diversity-Oriented Synthesis of Biaryl-Containing Medium Rings Using a One Bead/One Stock Solution Platform

4. Syntheses of Stereochemically Diverse Nine-Membered Ring-Containing Biaryls

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