Experimental and Computational Investigation of Facial Selectivity Switching in Nickel–Diamine–Acetate-Catalyzed Michael Reactions-Reference-Cited by-同舟云学术

Experimental and Computational Investigation of Facial Selectivity Switching in Nickel–Diamine–Acetate-Catalyzed Michael Reactions

Published:2023-02-22 Issue:12 Volume:88 Page:7764-7773
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sohtome Yoshihiro¹²^ORCID,Komagawa Shinsuke³^ORCID,Nakamura Ayako¹^ORCID,Hashizume Daisuke⁴^ORCID,Lectard Sylvain¹,Akakabe Mai¹²,Hamashima Yoshitaka¹^ORCID,Uchiyama Masanobu²³^ORCID,Sodeoka Mikiko¹²^ORCID

Affiliation:

1. Synthetic Organic Chemistry Laboratory, RIKEN Cluster for Pioneering Research, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan

2. RIKEN Center for Sustainable Resource Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan

3. Elements Chemistry Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama 351-0198, Japan

4. RIKEN Center for Emergent Matter Science, Wako, Saitama 351-0198, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02732

Reference56 articles.

1. Recent Developments in Enantioselective Nickel(II)-Catalyzed Conjugate Additions

2. Recent Advances in Catalytic Enantioselective Fluorination Reactions

3. Multiselective Catalytic Asymmetric Reactions Using α-Keto Esters as Pronucleophiles

4. Asymmetric Fluorination of α-Aryl Acetic Acid Derivatives with the Catalytic System NiCl2–Binap/R3SiOTf/2,6-Lutidine

5. Catalytic Asymmetric α-Chlorination of 3-Acyloxazolidin-2-one with a Trinary Catalytic System

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