B(C6F5)3-catalyzed stepwise 1,5-hydride migration/cyclization: diastereoselective construction of carbocyclic β-amino acid derivatives-Reference-Cited by-同舟云学术

B(C₆F₅)₃-catalyzed stepwise 1,5-hydride migration/cyclization: diastereoselective construction of carbocyclic β-amino acid derivatives

Published:2024 Issue:3 Volume:11 Page:864-870
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Zhiting¹,Liu Hongchi¹,Jiang Tianxiao¹,Huang Hanmin¹²^ORCID

Affiliation:

1. Key Laboratory of Precision and Intelligent Chemistry, and Department of Chemistry, University of Science and Technology of China, Hefei, 230026, P. R. China

2. Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education, Huaibei Normal University, Huaibei, 235000, P. R. China

Abstract

A stepwise 1,5-hydride migration/cyclization reaction enabled by B(C6F5)3 is established to deliver the corresponding six-membered carbocyclic β-amino acid derivatives with complete diastereoselectivity.

Funder

Chinese Academy of Sciences

National Key R&D Program of China

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01637D

Reference76 articles.