1094560-75-4Relevant academic research and scientific papers
A one-pot synthesis of (E,E)-1-Arylseleno-substituted 1,5-dien-3-ynes by palladium-catalysed three component cross-coupling reaction
Yao, Fang,Hao, Wenyan,Cai, Mingzhong
experimental part, p. 627 - 629 (2011/03/18)
(E,E)-1-Arylseleno-substituted 1,5-dien-3-ynes can be stereoselectively synthesised in one pot, in good yields with high stereoselectivity, by the Pd(PPh3)4-catalysed Stille coupling of (E)-1-iodo-2-arylselenoethenes with trimethylst
Stereoselective synthesis of (E,E)-1-arylseleno-substituted 1,5-dien-3-ynes
Rongli, Zhang,Minhua, Jiang,Mingzhong, Cai
experimental part, p. 101 - 103 (2009/07/18)
Sonogashira coupling of (E)-1-iodo-2-arylselenoethylenes 1 with (trimethylsilyl)acetylene gave (E)-1-arylseleno-4-(trimethylsilyl)but-1-en-3- ynes 2, which underwent desilylation to afford (E)-1-arylselenobut-1-en-3-ynes 3 in high yields. (E,E)-1-Arylsele
Facile stereoselective synthesis of (E)-1-arylseleno-substituted 1,3-enynes and their applications in synthesis of (E)-enediynes
Fang, Xiaoniu,Jiang, Minhua,Hu, Ronghua,Cai, Mingzhong
experimental part, p. 4170 - 4181 (2009/04/11)
(E)-1-Iodo-2-arylselenoethylenes 1 underwent the Sonogashira coupling reactions with terminal alkynes 2 to afford (E)-1-arylseleno-substituted 1,3-enynes 3 in high yields. (E)-1-Arylseleno-substituted 1,3-enynes 3 were coupled with alkynylmagnesium bromides 4 in the presence of a catalytic amount of NiCl2(PPh3)2 to give stereoselectively (E)-enediynes 5 in good yields. Copyright Taylor & Francis Group, LLC.
