Borylation of Aryl and Alkenyl Carbamates through Ni??Catalyzed C O Activation
K Huang, DG Yu, SF Zheng, ZH Wu…
Index: Huang, Kun; Yu, Da-Gang; Zheng, Shu-Fang; Wu, Zhen-Hua; Shi, Zhang-Jie Chemistry - A European Journal, 2011 , vol. 17, # 3 p. 786 - 791
Full Text: HTML
Citation Number: 64
Abstract
In the past several decades, Suzuki–Miyaura coupling has been well developed and has become one of the most useful tools to construct CÀC bond in both laboratory and industry.[1] As the major coupling partner of Suzuki–Miyaura coupling, aryl boronic acid and its derivatives showed their advantages due to the readily availability, low toxicity and high functional group tolerance.[2] Traditionally, they can be prepared by metal exchange from ...
Related Articles:
[Myslinska, Malgorzata; Heise, Glenn L.; Walsh, Dana J. Tetrahedron Letters, 2012 , vol. 53, # 24 p. 2937 - 2941]
[Yasuike, Shuji; Nakata, Kazuhide; Qin, Weiwei; Kaji, Toshiyuki; Kurita, Jyoji Chemistry Letters, 2006 , vol. 35, # 12 p. 1402 - 1403]
Borylation of organo halides and triflates using tetrakis (dimethylamino) diboron
[Bello, Charles S.; Schmidt-Leithoff, Joachim Tetrahedron Letters, 2012 , vol. 53, # 46 p. 6230 - 6235,6]
[Yasuike, Shuji; Nakata, Kazuhide; Qin, Weiwei; Kaji, Toshiyuki; Kurita, Jyoji Chemistry Letters, 2006 , vol. 35, # 12 p. 1402 - 1403]
[Yasuike, Shuji; Nakata, Kazuhide; Qin, Weiwei; Kaji, Toshiyuki; Kurita, Jyoji Chemistry Letters, 2006 , vol. 35, # 12 p. 1402 - 1403]