Optimized Synthetic Route for Enantioselective Preparation of (S)-Metolachlor from Commercially Available (R)-Propylene Oxide-Reference-Cited by-同舟云学术

Optimized Synthetic Route for Enantioselective Preparation of (S)-Metolachlor from Commercially Available (R)-Propylene Oxide

Published:2017-09-12 Issue:10 Volume:21 Page:1682-1688
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Yang Peng¹²,Wang Xiao¹²,Peng Lin¹,Chen Feng¹²,Tian Fang¹²,Tang Chao-Zhe¹,Wang Li-Xin¹^ORCID

Affiliation:

1. Key Laboratory of Asymmetric Synthesis and Chirotechnology of Sichuan Province, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, P. R. China

2. University of Chinese Academy of Sciences, Beijing 100049, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.7b00216

Reference46 articles.

1. Chiral Lewis base promoted trichlorosilane reduction of ketimines. An enantioselective organocatalytic synthesis of chiral amines

2. Chiral phosphine-phosphoramidite ligands for highly enantioselective hydrogenation of N-arylimines

3. Chiral Phosphine–Phosphoramidite Ligands for Highly Efficient Ir-Catalyzed Asymmetric Hydrogenation of Sterically Hindered N-Arylimines

4. Tunable ferrocenyl diphosphine ligands for the Ir-catalyzed enantioselective hydrogenation of N-aryl imines

5. Nucleophilic Aliphatic Substitution Reactions of Propachlor, Alachlor, and Metolachlor with Bisulfide (HS-) and Polysulfides (Sn2-)

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