中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
asymmetricsynthesisof35disubstitutedprolines

文献类型:期刊论文

作者Zhao L(赵亮); Zhou SB(周圣斌); Tong JH(童军华); Wang J(王江); Liu H(柳红)
刊名chinesejournaloforganicchemistry
出版日期2018
卷号38期号:6页码:1437
关键词BETA-AMINO ACIDS CHIRAL NICKEL(II) GLYCINATE MICHAEL ADDITION-REACTIONS ALPHA-AMINO EFFICIENT SYNTHESIS NI(II) COMPLEX KINETIC RESOLUTION ONE-POT NI(II)-COMPLEXES PYRROLIDINE 3,5-disubstituted proline Ni(II)-complex of glycine asymmetric Michael addition
ISSN号0253-2786
DOI10.6023/cjoc201712005
英文摘要Highly diastereoselective Michael addition reactions of chiral Ni(II)-complex of glycine with alpha,beta-unsaturated ketones in the presence of 1,8-diazabicyclo5.4.0undec-7-ene (DBU) and MeOH at ambient temperature were achieved. The operationally convenient procedure for preparation of the target products renders that this method is an attractive strategy for practical synthesis of 3,5-disubstituted prolines.
资助项目[National Natural Science Foundation of China] ; [Major Project of Chinese National Programs for Fundamental Research and Development] ; [Shanghai Science and Technology Development Fund]
语种英语
源URL[http://119.78.100.183/handle/2S10ELR8/285445]  
专题中国科学院上海药物研究所
作者单位中国科学院上海药物研究所
推荐引用方式
GB/T 7714
Zhao L,Zhou SB,Tong JH,et al. asymmetricsynthesisof35disubstitutedprolines[J]. chinesejournaloforganicchemistry,2018,38(6):1437.
APA 赵亮,周圣斌,童军华,王江,&柳红.(2018).asymmetricsynthesisof35disubstitutedprolines.chinesejournaloforganicchemistry,38(6),1437.
MLA 赵亮,et al."asymmetricsynthesisof35disubstitutedprolines".chinesejournaloforganicchemistry 38.6(2018):1437.

入库方式: OAI收割

来源:上海药物研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。