Organocatalytic Asymmetric Synthesis of Six-Membered Carbocycle-Based Spiro Compounds-Reference-Cited by-同舟云学术

Organocatalytic Asymmetric Synthesis of Six-Membered Carbocycle-Based Spiro Compounds

Published:2017-11-16 Issue:2 Volume:360 Page:194-228
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Xie Xin¹,Huang Wei²,Peng Cheng¹²,Han Bo¹

Affiliation:

1. State Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources; Chengdu University of Traditional Chinese Medicine; Chengdu 611137 People's Republic of China

2. Ministry of Education Key Laboratory of Standardization of Chinese Medicine, School of Pharmacy; Chengdu University of Traditional Chinese Medicine; Chengdu 611137 People's Republic of China

Funder

National Natural Science Foundation of China

Science & Technology Department of Sichuan Province

Foundation for the Authors of National Excellent Doctoral Dissertations of PR China

China Postdoctoral Science Foundation

Publisher

Wiley

Subject

General Chemistry

Reference240 articles.

1. Enantioselective methodologies for the synthesis of spiro compounds

2. Enantioselective Construction of Spiro[2H-pyran-3,4′-indoline] by a Systematic Michael/Reduction/Cyclization Sequence Triggered by the Asymmetric Conjugate Addition of Ketones to Isatylidenemalononitriles