Bifunctional tertiary amine-squaramide catalyzed asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides with oxindoles
Deng, Yu-Hua1,2; Zhang, Xiang-Zhi3; Yu, Ke-Yin3; Yan, Xu3; Du, Ji-Yuan3; Huang HM(黄汉民)1; Fan, Chun-An1,3
刊名Chemical Communications
2016
卷号52期号:22页码:4183-4186
ISSN号1359-7345
通讯作者Fan, Chun-An
英文摘要

The asymmetric catalytic 1,6-addition of p-QMs with racemic oxindoles under the bifunctional catalysis of C2-symmetric dimeric Cinchona-derived squaramide is described. This tertiary amine-squaramide catalyzed reaction provides a diastereoselective and enantioselective approach to the effective assembly of diverse diarylmethine-substituted oxindoles having vicinal tertiary and quaternary stereocenters.

学科主题物理化学与绿色催化
收录类别SCI
资助信息the NSFC (21572083;21322201;21290180);the FRFCU (lzujbky-2015-48);PCSIRT (IRT-15R28);the 111 Project of MOE of China (111-2-17);Chang Jiang Scholars Program (C.-A. F.)
语种英语
WOS记录号WOS:000372175700016
内容类型期刊论文
源URL[http://210.77.64.217/handle/362003/19787]  
专题兰州化学物理研究所_OSSO国家重点实验室
作者单位1.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, 222 Tianshui Nanlu, Lanzhou 730000, Peoples R China
推荐引用方式
GB/T 7714
Deng, Yu-Hua,Zhang, Xiang-Zhi,Yu, Ke-Yin,et al. Bifunctional tertiary amine-squaramide catalyzed asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides with oxindoles[J]. Chemical Communications,2016,52(22):4183-4186.
APA Deng, Yu-Hua.,Zhang, Xiang-Zhi.,Yu, Ke-Yin.,Yan, Xu.,Du, Ji-Yuan.,...&Fan, Chun-An.(2016).Bifunctional tertiary amine-squaramide catalyzed asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides with oxindoles.Chemical Communications,52(22),4183-4186.
MLA Deng, Yu-Hua,et al."Bifunctional tertiary amine-squaramide catalyzed asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides with oxindoles".Chemical Communications 52.22(2016):4183-4186.
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