1126896-41-0Relevant articles and documents
A Copper-Catalyzed Sonogashira Coupling Reaction of Diverse Activated Alkyl Halides with Terminal Alkynes Under Ambient Conditions
Cao, Yu-Xi,Dong, Xiao-Yang,Yang, Jun,Jiang, Sheng-Peng,Zhou, Shuangliu,Li, Zhong-Liang,Chen, Guo-Qiang,Liu, Xin-Yuan
, p. 2280 - 2284 (2020)
We describe a copper-catalyzed Sonogashira coupling reaction of alkyl halides with terminal alkynes under ambient conditions, efficiently providing a versatile tool for the construction of substituted alkynes. A new proline-based N,N,P-ligand is utilized to promote the transformation under a mild reaction condition. Diverse alkyl halides, such as primary and secondary (hetero)benzyl chlorides and bromides, secondary and tertiary α-bromo amides and propargylic bromide, are applicable to provide a wide array of alkynes. (Figure presented.).
Fe(OTf)3-catalyzed addition of sp C-H bonds to olefins
Kohno, Kazufumi,Nakagawa, Kou,Yahagi, Takeshi,Choi, Jun-Chul,Yasuda, Hiroyuki,Sakakura, Toshiyasu
experimental part, p. 2784 - 2785 (2009/07/30)
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