Novel α-arylnitriles synthesis via Ni-catalyzed cross-coupling of α-bromonitriles with arylboronic acids under mild conditions
Yang YY(杨莹莹) ; Tang S(唐山) ; Liu C(刘超) ; Zhang HM(张惠敏) ; Sun ZX(孙哲逊) ; Lei AW(雷爱文)
刊名Org. Biomol. Chem.
2011
卷号9页码:5343-5345
ISSN号1477-0520
通讯作者雷爱文
中文摘要An applicable and easy-handling Ni-catalyst can be used to promote direct arylation of a-bromonitriles with various arylboronic acids to construct a-arylnitriles undermild conditions. The methodology tolerates b-hydrogens and functional groups in the substrates.
学科主题物理化学
收录类别SCI
资助信息the National Natural Science Foundation of China (21025206;20832003;20972118;20772093);the “973” Project from the MOST of China (2011CB808600);“the Fundamental Research Funds for the Central Universities”;Program for New Century Excellent Talents in University (NCET)
语种英语
公开日期2012-09-20
内容类型期刊论文
源URL[http://210.77.64.217/handle/362003/394]  
专题兰州化学物理研究所_OSSO国家重点实验室
推荐引用方式
GB/T 7714
Yang YY,Tang S,Liu C,et al. Novel α-arylnitriles synthesis via Ni-catalyzed cross-coupling of α-bromonitriles with arylboronic acids under mild conditions[J]. Org. Biomol. Chem.,2011,9:5343-5345.
APA 杨莹莹,唐山,刘超,张惠敏,孙哲逊,&雷爱文.(2011).Novel α-arylnitriles synthesis via Ni-catalyzed cross-coupling of α-bromonitriles with arylboronic acids under mild conditions.Org. Biomol. Chem.,9,5343-5345.
MLA 杨莹莹,et al."Novel α-arylnitriles synthesis via Ni-catalyzed cross-coupling of α-bromonitriles with arylboronic acids under mild conditions".Org. Biomol. Chem. 9(2011):5343-5345.
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