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Enantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral beta-Alkyl-beta-aryl Amino Alcohols
Alternative TitleEnantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral beta-Alkyl-beta-aryl Amino Alcohols
Chen YJ(陈亚静); Chen YH(陈亚恒); Feng CG(冯陈国); Lin GQ(林国强)
2014
Source PublicationOrg. Lett.
Volume16Issue:12Pages:3400-3403
AbstractThe enantioselective rhodium-catalyzed 1,2-addition of arylboronates to cyclic N-sulfamidate alkylketimines was developed. With a rhodium/diene complex as catalyst, high enantioselectivity and broad functional group tolerance were observed. The resulting sulfamidates can easily be converted into chiral beta-alkyl-beta-aryl amino alcohols.
Subject Area天然产物有机化学
DOI10.1021/ol501464e
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Indexed BySCI
Language英语
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Cited Times:44[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38984
Collection中科院天然产物有机化学重点实验室
Corresponding AuthorFeng CG(冯陈国); Lin GQ(林国强)
Affiliation中科院上海有机化学研究所
Recommended Citation
GB/T 7714
Chen YJ,Chen YH,Feng CG,et al. Enantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral beta-Alkyl-beta-aryl Amino Alcohols[J]. Org. Lett.,2014,16(12):3400-3403.
APA 陈亚静,陈亚恒,冯陈国,&林国强.(2014).Enantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral beta-Alkyl-beta-aryl Amino Alcohols.Org. Lett.,16(12),3400-3403.
MLA 陈亚静,et al."Enantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral beta-Alkyl-beta-aryl Amino Alcohols".Org. Lett. 16.12(2014):3400-3403.
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