中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Copper-Catalyzed Addition of Alkylboranes to Iminoacetates: Access to alpha-Alkyl Branched alpha-Amino Acids

文献类型:期刊论文

作者Jiang, HF; Zeng, W; Xiao, XS; Zhang, W; Lu, XX; Deng, YF; Zeng, W (reprint author), South China Univ Technol, Sch Chem & Chem Engn, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510641, Guangdong, Peoples R China.
刊名ADVANCED SYNTHESIS & CATALYSIS
出版日期2016
卷号358期号:15页码:2497-2509
关键词Alkylboranes A-amino Acids Copper Catalysis Imino Esters Unactivated Monoalkenes
DOI10.1002/adsc.201600248
产权排序2
文献子类Article
英文摘要A copper(I)-catalyzed addition of alkylborane reagents to alpha-iminoacetates has been developed to assemble both acyclic and cyclic alpha-branched alpha-amino carboxylic acid derivatives in good yields. A wide variety of unactivated alkenes are well tolerated in this transformation.
学科主题Chemistry
语种英语
资助机构NSFC [21372085] ; NSFC [21372085] ; Science and Technology Program of Guangzhou [156300075] ; Science and Technology Program of Guangzhou [156300075] ; NSFC [21372085] ; NSFC [21372085] ; Science and Technology Program of Guangzhou [156300075] ; Science and Technology Program of Guangzhou [156300075]
源URL[http://210.75.237.14/handle/351003/28183]  
专题成都生物研究所_天然产物研究
通讯作者Zeng, W (reprint author), South China Univ Technol, Sch Chem & Chem Engn, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510641, Guangdong, Peoples R China.
推荐引用方式
GB/T 7714
Jiang, HF,Zeng, W,Xiao, XS,et al. Copper-Catalyzed Addition of Alkylboranes to Iminoacetates: Access to alpha-Alkyl Branched alpha-Amino Acids[J]. ADVANCED SYNTHESIS & CATALYSIS,2016,358(15):2497-2509.
APA Jiang, HF.,Zeng, W.,Xiao, XS.,Zhang, W.,Lu, XX.,...&Zeng, W .(2016).Copper-Catalyzed Addition of Alkylboranes to Iminoacetates: Access to alpha-Alkyl Branched alpha-Amino Acids.ADVANCED SYNTHESIS & CATALYSIS,358(15),2497-2509.
MLA Jiang, HF,et al."Copper-Catalyzed Addition of Alkylboranes to Iminoacetates: Access to alpha-Alkyl Branched alpha-Amino Acids".ADVANCED SYNTHESIS & CATALYSIS 358.15(2016):2497-2509.

入库方式: OAI收割

来源:成都生物研究所

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