New Mechanism for Cinchona Alkaloid-Catalysis Allows for an Efficient Thiophosphorylation Reaction-Reference-Cited by-同舟云学术

New Mechanism for Cinchona Alkaloid-Catalysis Allows for an Efficient Thiophosphorylation Reaction

Published:2020-11-12 Issue:47 Volume:142 Page:20021-20029
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Salehi Marzijarani Nastaran¹^ORCID,Lam Yu-hong²^ORCID,Wang Xiao³^ORCID,Klapars Artis¹,Qi Ji¹⁴^ORCID,Song Zhiyan⁵,Sherry Benjamin D.¹,Liu Zhijian¹^ORCID,Ji Yining¹^ORCID

Affiliation:

1. Department of Process Research and Development, Merck & Co., Inc., Rahway, New Jersey 07065, United States

2. Department of Computational and Structural Chemistry, Merck & Co., Inc., Rahway, New Jersey 07065, United States

3. Department of Analytical Research and Development, Merck & Co., Inc., Rahway, New Jersey 07065, United States

4. Department of Process Research and Development, MSD R&D (China) Co., Ltd., Building 21 Rongda Road, Wangjing R&D Base, Zhongguancun Electronic Zone West Zone, Beijing 100012, China

5. Department of Synthetic Chemistry, Pharmaron Beijing Co., Ltd., 6 Taihe Road BDA, Beijing 100176, 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.0c09192

Reference78 articles.

1. Organocatalysis

2. Bifunctional organocatalysts for the asymmetric synthesis of axially chiral benzamides

3. Highly Enantioselective Conjugate Addition of Malonate and β-Ketoester to Nitroalkenes: Asymmetric C−C Bond Formation with New Bifunctional Organic Catalysts Based on Cinchona Alkaloids

4. Asymmetric Catalysis by Chiral Hydrogen-Bond Donors

5. Asymmetric Organic Catalysis with Modified Cinchona Alkaloids

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