LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Novel α-arylnitriles synthesis via Ni-catalyzed cross-coupling of α-bromonitriles with arylboronic acids under mild conditions
Department羰基合成与选择氧化国家重点实验室
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)
2011
Source PublicationOrg. Biomol. Chem.
ISSN1477-0520
Volume9Pages:5343-5345
AbstractAn 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.
Subject Area物理化学
Funding Organizationthe 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)
Indexed BySCI
Language英语
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/394
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorLei AW(雷爱文)
Recommended Citation
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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