版权说明 操作指南
首页 > 成果 > 详情

Palladium-catalyzed C-H acetoxylation of 2-methoxyimino-2-aryl-acetates and acetamides

认领
导出
Link by 万方学术期刊
反馈
分享
QQ微信 微博
成果类型:
期刊论文
作者:
Wang, Liang;Xia, Xu-Dong;Guo, Wei;Chen, Jia-Rong;Xiao, Wen-Jing*
通讯作者:
Xiao, Wen-Jing
作者机构:
[Xia, Xu-Dong; Guo, Wei; Xiao, Wen-Jing; Chen, Jia-Rong; Wang, Liang] Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China.
[Xiao, Wen-Jing] Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China.
通讯机构:
[Xiao, Wen-Jing] C
Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China.
语种:
英文
期刊:
Organic & Biomolecular Chemistry
ISSN:
1477-0520
年:
2011
卷:
9
期:
20
页码:
6895-6898
基金类别:
National Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [20872043, 21072069, 21002036]; National Basic Research Program of ChinaNational Basic Research Program of China [2011CB808600]; Program for Changjiang Scholars and Inovation Research Team in UniversityProgram for Changjiang Scholars & Innovative Research Team in University (PCSIRT) [IRT0953]
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
Palladium-catalyzed C-H acetoxylation reactions of 2-methoxyimino-2-aryl- acetates and acetamides have been developed. These transformations feature excellent regioselectivity, wide substrate scope, and moderate to good yields. The product can be easily converted into naturally unprecedented α-amino acids in excellent yields. &c...

反馈

验证码:
看不清楚,换一个
确定
取消

成果认领

标题:
用户 作者 通讯作者
请选择
请选择
确定
取消

提示

该栏目需要登录且有访问权限才可以访问

如果您有访问权限,请直接 登录访问

如果您没有访问权限,请联系管理员申请开通

管理员联系邮箱:yun@hnwdkj.com