Enantioselective Synthesis of Axially Chiral Sulfone-Containing Styrenes Based on Ion-Exchange Strategy-Reference-Cited by-同舟云学术

Enantioselective Synthesis of Axially Chiral Sulfone-Containing Styrenes Based on Ion-Exchange Strategy

Published:2024-04-25 Issue:17 Volume:26 Page:3498-3502
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lian Peng-Fei¹,Wang Ying²,Li Zi-Hao¹,Zhang Shu-Yu¹^ORCID,Duan Abing²^ORCID,Bai He-Yuan¹³^ORCID

Affiliation:

1. Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, and School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China

2. College of Environmental Science and Engineering, Hunan University, Changsha 410082, P. R. China

3. Chongqing Research Institute, Shanghai Jiao Tong University, Chongqing 401120, China

Funder

National Key Research and Development Program of China

Natural Science Foundation of Chongqing Municipality

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00704

Reference41 articles.

1. Rational design, enantioselective synthesis and catalytic applications of axially chiral EBINOLs

2. Synthesis of Axially Chiral Styrenes through Pd‐Catalyzed Asymmetric C−H Olefination Enabled by an Amino Amide Transient Directing Group

3. Atroposelective Access to Oxindole-Based Axially Chiral Styrenes via the Strategy of Catalytic Kinetic Resolution

4. Atroposelective Synthesis of Conjugated Diene-Based Axially Chiral Styrenes via Pd(II)-Catalyzed Thioether-Directed Alkenyl C–H Olefination

5. Rational Design of Axially Chiral Styrene‐Based Organocatalysts and Their Application in Catalytic Asymmetric (2+4) Cyclizations