Enantioselective Dearomatization of Indoles via SmI<sub>2</sub>-Mediated Intermolecular Reductive Coupling with Ketones-Reference-Cited by-同舟云学术

Enantioselective Dearomatization of Indoles via SmI₂-Mediated Intermolecular Reductive Coupling with Ketones

Published:2023-04-26 Issue:18 Volume:145 Page:10314-10321
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhang Wen-Yun¹,Wang Hu-Chong¹,Wang Ye¹,Zheng Chao¹^ORCID,You Shu-Li¹²^ORCID

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China

2. New Cornerstone Science Laboratory, Shanghai 200032, China

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

Chinese Academy of Sciences

New Cornerstone Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.3c01994

Reference86 articles.

1. bKagan, H. B.; Namy, J. L. InLanthanides: Chemistry and Use in Organic Synthesis; Kobayashi, S., Ed. Springer: New York, 1999; p 155.

2. SmI2-induced reductive cyclizations for the synthesis of cyclic ethers and applications in natural product synthesis

3. Samarium diiodide induced ketyl-(het)arene cyclisations towards novel N-heterocycles

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