Iron-Catalyzed Reductive Cyclization of o-Nitrostyrenes Using Phenylsilane as the Terminal Reductant-Reference-Cited by-同舟云学术

Iron-Catalyzed Reductive Cyclization of o-Nitrostyrenes Using Phenylsilane as the Terminal Reductant

Published:2017-07-24 Issue:8 Volume:7 Page:5518-5522
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Shevlin Michael¹²^ORCID,Guan Xinyu²,Driver Tom G.²³^ORCID

Affiliation:

1. Department of Process Research & Development, Merck & Co., Inc., 126 East Lincoln Avenue, Rahway, New Jersey 07065, United States

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

3. Institute of Next Generation Matter Transformation, College of Chemical Engineering, Huaqiao University, 668 Jimei Boulevard, Xiamen, Fujian 361021, People’s Republic of China

Funder

Division of Chemistry

University of Illinois at Chicago

Fujian Province

Office of the Vice-Chancellor of Research, Huaqiao University

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.7b01915

Reference71 articles.

1. aBoyer, J. H.InNitrenes;Lwowski, W., Ed.Wiley:New York, 1970; pp163–184.

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

3. Synthesis of Heterocycles via Intramolecular Annulation of Nitrene Intermediates

4. aBarden, T. C.InHeterocyclic Scaffolds II: Reactions and Applications of Indoles;Gribble, G. W., Ed.Springer:Berlin, Heidelberg, 2011; pp31–46.

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