Iridium-Catalyzed Double Asymmetric Hydrogenation of 2,5-Dialkylienecyclopentanones for the Synthesis of Chiral Cyclopentanones-Reference-Cited by-同舟云学术

Iridium-Catalyzed Double Asymmetric Hydrogenation of 2,5-Dialkylienecyclopentanones for the Synthesis of Chiral Cyclopentanones

Published:2022-10-20 Issue:43 Volume:24 Page:7878-7882
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Nie Yu¹,Yuan Qianjia¹,Gao Feng¹,Terada Masahiro²^ORCID,Zhang Wanbin¹^ORCID

Affiliation:

1. Shanghai Key Laboratory of Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P. R. China

2. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan

Funder

Ministry of Science and Technology of the People's Republic of China

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c02656

Reference43 articles.

1. Pyrrolidine-3-carboxylic Acids as Endothelin Antagonists. 2. Sulfonamide-Based ETA/ETB Mixed Antagonists

2. Structure-Activity Relationships of Enantiomers of the Azole Fungicide Ipconazole and Its Related Compounds

3. Aldose reductase from Schistosoma japonicum: crystallization and structure-based inhibitor screening for discovering antischistosomal lead compounds

4. Alkylaluminum halide induced cyclization of unsaturated carbonyl compounds

5. (2R,5R)-(-)-2,5-Dimethylcyclopentanone and (5S)-(+)-2,5-dimethyl-2-cyclopenten-1-one by microbiological reduction of racemic 2,5-dimethyl-2-cyclopenten-1-one

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