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	Why different ligands can control stereochemistry selectivity of Ni-catalyzed Suzuki-Miyaura cross-coupling of benzylic carbamates with arylboronic esters: a mechanistic study
	Xie, Hujun[1]; Li, Yang[1]; Wang, Lihong[1]; Kuang, Jian[1]; Lei, Qunfang[2]; Fang, Wenjun[2]
	2017
卷号	46期号:38页码:13010
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/5538833
专题	浙江工商大学
作者单位	1.[1]Zhejiang Gongshang Univ, Dept Appl Chem, 18 Xuezheng St, Hangzhou 310018, Zhejiang, Peoples R China 2.[2]Zhejiang Univ, Dept Chem, 38 Zheda Rd, Hangzhou 310027, Zhejiang, Peoples R China
推荐引用方式 GB/T 7714	Xie, Hujun[1],Li, Yang[1],Wang, Lihong[1],et al. Why different ligands can control stereochemistry selectivity of Ni-catalyzed Suzuki-Miyaura cross-coupling of benzylic carbamates with arylboronic esters: a mechanistic study[J],2017,46(38):13010.
APA	Xie, Hujun[1],Li, Yang[1],Wang, Lihong[1],Kuang, Jian[1],Lei, Qunfang[2],&Fang, Wenjun[2].(2017).Why different ligands can control stereochemistry selectivity of Ni-catalyzed Suzuki-Miyaura cross-coupling of benzylic carbamates with arylboronic esters: a mechanistic study.,46(38),13010.
MLA	Xie, Hujun[1],et al."Why different ligands can control stereochemistry selectivity of Ni-catalyzed Suzuki-Miyaura cross-coupling of benzylic carbamates with arylboronic esters: a mechanistic study".46.38(2017):13010.

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