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学科主题: 天然产物有机化学
题名: Enantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral beta-Alkyl-beta-aryl Amino Alcohols
其他题名: Enantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral beta-Alkyl-beta-aryl Amino Alcohols
作者: Chen YJ(陈亚静); Chen YH(陈亚恒); Feng CG(冯陈国); Lin GQ(林国强)
通讯作者: 冯陈国 ; 林国强
刊名: Org. Lett.
发表日期: 2014
DOI: 10.1021/ol501464e
卷: 16, 期:12, 页:3400-3403
收录类别: SCI
英文摘要: The 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.
语种: 英语
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/38984
Appears in Collections:中科院天然产物有机化学重点实验室_期刊论文

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作者单位: 中科院上海有机化学研究所

Recommended Citation:
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.
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