Lewis Basic Selenium Catalyzed Chloroamidation of Olefins Using Nitriles as the Nucleophiles-Reference-Cited by-同舟云学术

Lewis Basic Selenium Catalyzed Chloroamidation of Olefins Using Nitriles as the Nucleophiles

Published:2013-03-05 Issue:6 Volume:15 Page:1310-1313
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tay Daniel Weiliang¹,Tsoi Ivan Tan¹,Er Jun Cheng¹,Leung Gulice Yiu Chung¹,Yeung Ying-Yeung¹

Affiliation:

1. Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, and A*STAR−Institute of Chemical & Engineering Sciences, 11 Biopolis Way, Helios, #03-08, Singapore 138667

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol400249x

Reference52 articles.

1. aKemp, J. E. G.InComprehensive Organic Synthesis;Trost, B. M., Fleming, I., Eds.Pergamon:Oxford, 1991; Vol.3, pp471–513and references cited therein.

2. Total synthesis of allosamidin: an application of the sulfonamidoglycosylation of glycals

3. The chromous chloride promoted addition of N-haloamides to olefins. V. The addition of N-chloroamides to enol ethers: synthesis of acyloxy and acyl derivatives of α-amino acetals and ketals (aldehydes and ketones) and of 2-amino sugars

4. Addition of N,N-dichlorosulfonamides to unsaturates

5. Stereoselective synthesis of protected amines and diamines from alkenes using N,N-Dichloro-t-butylcarbamate

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