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Catalytic Asymmetric [4 + 1] Annulation of Sulfur Ylides with Copper-Allenylidene Intermediates

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成果类型:
期刊论文
作者:
Wang, Qiang;Li, Tian-Ren;Lu, Liang-Qiu*;Li, Miao-Miao;Zhang, Kai;...
通讯作者:
Lu, Liang-Qiu;Xiao, Wen-Jing
作者机构:
[Lu, LQ; Xiao, WJ; Lu, Liang-Qiu; Li, Tian-Ren; Xiao, Wen-Jing; Li, Miao-Miao; Wang, Qiang; Zhang, Kai] Cent China Normal Univ, Coll Chem, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China.
[Xiao, Wen-Jing] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China.
通讯机构:
[Lu, LQ; Xiao, WJ] C
[Xiao, Wen-Jing] L
Cent China Normal Univ, Coll Chem, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China.
Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China.
语种:
英文
期刊:
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN:
0002-7863
年:
2016
卷:
138
期:
27
页码:
8360-8363
基金类别:
We are grateful to the National Natural Science Foundation of China (Nos. 21232003, 21472057, and 21572074) and other financial support (Nos. 201422, CCNU15A02007, and 2015CFA033) for this research.
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
The first copper-catalyzed asymmetric decarboxylative [4 + 1] cycloaddition of propargylic carbamates and sulfur ylides was successfully developed. This strategy led to a series of chiral indolines with synthetically flexible alkyne groups in good yields and with high enantio- and diastereoselectivities (up to 99% yield, 98% ee, and >95:5 dr). A possible mechanism and stereoinduction mode with copper-allenylidenes w...

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