84553-28-6Relevant academic research and scientific papers
Transition-Metal-Free One-Step Synthesis of Ynamides
Zeng, Xianzhu,Tu, Yongliang,Zhang, Zhenming,You, Changming,Wu, Jiao,Ye, Zhiying,Zhao, Junfeng
, p. 4458 - 4466 (2019/03/26)
A robust transition-metal-free one-step strategy for the synthesis of ynamides from sulfonamides and (Z)-1,2-dichloroalkenes or alkynyl chlorides is presented. This method is not only effective for internal ynamides but also amenable for terminal ynamides. Various functional groups, even the vinyl moiety, are compatible, and thus, this strategy offers the opportunity for further functionalization.
Highly stereoselective synthesis of (Z)-1,2-dihaloalkenes by a Pd-catalyzed hydrohalogenation of alkynyl halides
Zhu, Gangguo,Chen, Dongxu,Wang, Yuyi,Zheng, Renwei
supporting information; experimental part, p. 5796 - 5798 (2012/07/28)
An unprecedented Pd-catalyzed hydrohalogenation of alkynyl halides for the regio- and stereoselective synthesis of (Z)-1,2-dihaloalkenes has been realized using [(allyl)PdCl]2 as the catalyst and cis,cis-1,5-cyclooctadiene as the ligand. The advantages of this protocol are well illustrated by the assembly of trisubstituted (Z)-enynes and multifunctional benzenes via iterative cross-coupling reactions or tandem Diels-Alder-aromatization reactions, respectively.
REACTION DE L'ACIDE PERCHLORIQUE SUR LES PHENYLACETYLENES SUBSTITUES. MISE EN EVIDENCE D'UN MECANISME IONIQUE ET RADICALAIRE
Montheard, Jean-Pierre,Camps, Marcel,Benzaid, Ahmed,Pascal, Jean-Louis
, p. 3483 - 3486 (2007/10/02)
We have studied the reaction of perchloric acid in acetic acid medium on some substituted phenylacetylenes.The ionic and radicalar mechanism is in agreement with the formation of and alkenyl perchlorate which is decomposed according to an homolytic process.
