Catalytic asymmetric Michael and Nef-type sequential reaction of nitroolefin with azlactone to construct oxazole-fused succinimide.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
25 Oct 2024
Historique:
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

A series of oxazole-fused succinimides bearing vicinal quaternary carbon centers were synthesized. This process takes place between nitroolefins and azlactones in the presence of a bifunctional chiral guanidine-sulfonamide organocatalyst, followed by a Nef-type transformation under the treatment of DMAP/Ac

Identifiants

pubmed: 39450603
doi: 10.1039/d4cc04858j
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Rui Weng (R)

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China. liuxh@scu.edu.cn.

Yuqiao Zhou (Y)

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China. liuxh@scu.edu.cn.

Yaqin Zhang (Y)

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China. liuxh@scu.edu.cn.

Xiaoming Feng (X)

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China. liuxh@scu.edu.cn.

Xiaohua Liu (X)

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China. liuxh@scu.edu.cn.

Classifications MeSH