In situ generation of N-unsubstituted imines from alkyl azides and their applications for imine transfer via copper catalysis-Reference-Cited by-同舟云学术

In situ generation of N-unsubstituted imines from alkyl azides and their applications for imine transfer via copper catalysis

Published:2017-08-04 Issue:8 Volume:3 Page:
ISSN:2375-2548
Container-title:Science Advances
language:en
Short-container-title:Sci. Adv.

Author:

Hu Lu¹,Liu Yahu A.²,Liao Xuebin¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, China.

2. Medicinal Chemistry, Genomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.

Abstract

Multisubstituted pyridines or indoles were synthesized using N-unsubstituted imines in situ–generated from alkyl azides.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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5. Iron(II) bromide-catalyzed intramolecular C−H bond amination–[1,2]-shift tandem reactions of aryl azides;Nguyen Q.;J. Am. Chem. Soc.,2013

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