asymmetricsynthesisof35disubstitutedprolines

doi:10.6023/cjoc201712005

	asymmetricsynthesisof35disubstitutedprolines
	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
	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
DOI	10.6023/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
内容类型	期刊论文
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.