Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates-Reference-Cited by-同舟云学术

Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates

Published:2015-12-02 Issue:24 Volume:17 Page:6046-6049
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Douchez Antoine¹,Lubell William D.¹

Affiliation:

1. Département de Chimie, Université de Montréal, C.P. 6128, Succursale Centre-Ville, Montréal H3C 3J7, Canada

Funder

Canadian Institutes of Health Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b03046

Reference34 articles.

1. The benzodiazepine story

2. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures

3. Privileged Structures as Leads in Medicinal Chemistry

4. 1,4-benzodiazepin-2-ones in medicinal chemistry

5. Modular Synthesis of Cyclic Peptidomimetics Inspired by γ-Turns

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