Highly Regio- and Enantioselective Alkoxycarbonylative Amination of Terminal Allenes Catalyzed by a Spiroketal-Based Diphosphine/Pd(II) Complex-Reference-Cited by-同舟云学术

Highly Regio- and Enantioselective Alkoxycarbonylative Amination of Terminal Allenes Catalyzed by a Spiroketal-Based Diphosphine/Pd(II) Complex

Published:2015-09-23 Issue:49 Volume:137 Page:15346-15349
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liu Jiawang¹,Han Zhaobin¹,Wang Xiaoming¹,Wang Zheng¹,Ding Kuiling¹²

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

2. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China

Funder

Chinese Academy of Sciences

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.5b07764

Reference49 articles.

1. Modern Allene Chemistry

2. Palladium-Catalyzed Reactions of Allenes

3. Three Carbons for Complexity! Recent Developments of Palladium-Catalyzed Reactions of Allenes

4. Transition metal-catalyzed three-component coupling of allenes and the related allylation reactions

5. Intramolecular Palladium(II)-Catalyzed 1,2-Addition to Allenes

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