Asymmetric [3 + 1]-Cycloaddition Reaction via Diazo Discrimination.


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
01 Oct 2021
Historique:
pubmed: 14 9 2021
medline: 14 9 2021
entrez: 13 9 2021
Statut: ppublish

Résumé

The enantioselective [3 + 1]-cycloaddition of two structurally different diazo compounds has been achieved using chiral bisoxazoline copper(I) complexes as a catalyst, providing a novel route for the synthesis of cyclobutenes containing a quaternary stereocenter. Typically, this reaction represents the first example of asymmetric cross-electrophile coupling of two diazo substrates via carbene discrimination.

Identifiants

pubmed: 34510903
doi: 10.1021/acs.orglett.1c02825
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7613-7617

Auteurs

Yong Xu (Y)

Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164, P. R. China.

Zhen Wang (Z)

Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164, P. R. China.

Jiangtao Sun (J)

Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164, P. R. China.

Classifications MeSH