Highly enantio-selective synthesis of aza-spirocyclic indanones via rhodium catalysis†

IF 2.9 3区化学 Q1 CHEMISTRY, ORGANIC

Organic & Biomolecular Chemistry Pub Date : 2025-03-12 DOI:10.1039/D5OB00291E

Cai-Lan Kou, Long Yang, Ling-Zhi Sun, Meng Li, Xi Luo, Hong-Bo Guo and Jian-Bo Xie

引用次数: 0

Abstract

A facile synthetic method for chiral aza-spirocyclic indanones was developed with excellent enantioselectivities (81%–98% ee) via rhodium-catalyzed asymmetric domino conjugate addition/1,4-Rh shift/nucleophilic addition with traditional substrates of conjugate addition. The factors that affected the selectivity for aza-spirocyclic indanones were systematically studied.

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来源期刊

Organic & Biomolecular Chemistry 化学-有机化学

CiteScore

5.50

自引率

9.40%

发文量

1056

审稿时长

1.3 months

期刊介绍： Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.