Computational Study on the Mechanism and Origin of the Regioselectivity and Stereospecificity in Pd/SIPr-Catalyzed Ring-Opening Cross-Coupling of 2-Arylaziridines with Arylboronic Acids-Reference-Cited by-同舟云学术

Computational Study on the Mechanism and Origin of the Regioselectivity and Stereospecificity in Pd/SIPr-Catalyzed Ring-Opening Cross-Coupling of 2-Arylaziridines with Arylboronic Acids

Published:2019-03-26 Issue:5 Volume:9 Page:4582-4592
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Sharma Akhilesh K.¹^ORCID,Sameera W. M. C.²^ORCID,Takeda Youhei³^ORCID,Minakata Satoshi³^ORCID

Affiliation:

1. Fukui Institute for Fundamental Chemistry, Kyoto University, Takano-Nishishiraki-cho, 34-4, Sakyo-ku, Kyoto 606-8103, Japan

2. Institute of Low Temperature Science, Hokkaido University, Sapporo, Hokkaido 060-0819, Japan

3. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamadaoka 2-1, Suita, Osaka 565-0871, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.9b01191

Reference87 articles.

1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

2. Recent Synthetic Applications of Chiral Aziridines

3. Nucleophilic ring opening of aziridines

4. Recent developments in regioselective ring opening of aziridines

5. Regioselectivity in the ring opening of non-activated aziridines

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