Literature DB >> 21626595

Catalytic enantioselective Henry reactions of isatins: application in the concise synthesis of (S)-(-)-spirobrassinin.

Lu Liu1, Shilei Zhang, Fei Xue, Guangshun Lou, Haoyi Zhang, Shichao Ma, Wenhu Duan, Wei Wang.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2011        PMID： 21626595     DOI： 10.1002/chem.201101025

Source DB:  PubMed          Journal:  Chemistry        ISSN： 0947-6539            Impact factor:   5.236


× No keyword cloud information.
  5 in total

1.  Enantioselective and regioselective indium(III)-catalyzed addition of pyrroles to isatins.

Authors:  Elisa G Gutierrez; Casey J Wong; Aziza H Sahin; Annaliese K Franz
Journal:  Org Lett       Date:  2011-10-11       Impact factor: 6.005

2.  Organocatalytic asymmetric Michael addition of unprotected 3-substituted oxindoles to 1,4-naphthoquinone.

Authors:  Jin-Sheng Yu; Feng Zhou; Yun-Lin Liu; Jian Zhou
Journal:  Beilstein J Org Chem       Date:  2012-08-23       Impact factor: 2.883

3.  Catalytic enantioselective radical coupling of activated ketones with N-aryl glycines.

Authors:  Yang Liu; Xiangyuan Liu; Jiangtao Li; Xiaowei Zhao; Baokun Qiao; Zhiyong Jiang
Journal:  Chem Sci       Date:  2018-08-27       Impact factor: 9.825

4.  Cu (II)-catalyzed asymmetric henry reaction with a novel C1-symmetric aminopinane-derived ligand.

Authors:  Liudmila Filippova; Yngve Stenstrøm; Trond Vidar Hansen
Journal:  Molecules       Date:  2015-04-09       Impact factor: 4.411

5.  Organocatalytic asymmetric Henry reaction of 1H-pyrrole-2,3-diones with bifunctional amine-thiourea catalysts bearing multiple hydrogen-bond donors.

Authors:  Ming-Liang Zhang; Deng-Feng Yue; Zhen-Hua Wang; Yuan Luo; Xiao-Ying Xu; Xiao-Mei Zhang; Wei-Cheng Yuan
Journal:  Beilstein J Org Chem       Date:  2016-02-16       Impact factor: 2.883
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.