Diborane-Mediated Deoxygenation of o-Nitrostyrenes To Form Indoles-Reference-Cited by-同舟云学术

Diborane-Mediated Deoxygenation of o-Nitrostyrenes To Form Indoles

Published:2016-08-08 Issue:16 Volume:18 Page:4088-4091
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yang Kai¹,Zhou Fei²,Kuang Zhijie¹,Gao Guoliang¹,Driver Tom G.¹²,Song Qiuling¹

Affiliation:

1. Institute of Next Generation Matter Transformation, College of Chemical Engineering, College of Material Sciences Engineering at Huaqiao University, 668 Jimei Boulevard, Xiamen, Fujian 361021, P. R. China

2. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061, United States

Funder

National Science Foundation of Fujian Province

Fujian Hundred Talents Plan

Recruitment Program of Global Experts (1000 Talents Plan),

the National Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b01934

Reference82 articles.

1. aBoyer, J. H.Nitrenes;Wiley:New York, 1970; p163.

2. bSundberg, R. J.InComprehensive Heterocyclic Chemistry;Katritzky, A., Rees, C. W., Scriven, E. F. V., Eds.Pergamon:New York, 1996; Vol.2, pp119–206.

3. Synthesis of Heterocycles via Intramolecular Annulation of Nitrene Intermediates

4. Indole synthesis: a review and proposed classification

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