Organocatalytic [3+2] Cycloadditions of Barbiturate-Based Olefins with 3-Isothiocyanato Oxindoles: Highly Diastereoselective and Enantioselective Synthesis of Dispirobarbiturates-Reference-Cited by-同舟云学术

Organocatalytic [3+2] Cycloadditions of Barbiturate-Based Olefins with 3-Isothiocyanato Oxindoles: Highly Diastereoselective and Enantioselective Synthesis of Dispirobarbiturates

Published:2016-07-13 Issue:16 Volume:358 Page:2619-2630
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Zhao Hong-Wu¹,Tian Ting¹,Pang Hai-Liang¹,Li Bo¹,Chen Xiao-Qin¹,Yang Zhao¹,Meng Wei¹,Song Xiu-Qing¹,Zhao Yu-Di¹,Liu Yue-Yang¹

Affiliation:

1. College of Life Science and Bio-engineering; Beijing University of Technology; Beijing 100124 People's Republic of China

Funder

Beijing Municipal Commission of Education

Beijing Municipal Natural Science Foundation

Basic Research Foundation of Beijing University of Technology

Funding Project for Academic Human Resources Development in Institutions of Higher Learning Under the Jurisdiction of Beijing Municipality

Doctoral Scientific Research Start-up Foundation of Beijing University of Technology

Publisher

Wiley

Subject

General Chemistry

Reference52 articles.

1. Silicon Heterocyclic Compounds. III. Silicon-Substituted Spirobarbiturates1

2. Anticonvulsant and sedative effects of some 5-substituted bromopyrazolinic spirobarbiturates

3. Structure-based design of potent and selective inhibitors of collagenase-3 (MMP-13)

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