131569-81-8Relevant articles and documents
Borylstannylation of alkynes with inverse regioselectivity: Copper-catalyzed three-component coupling using a masked diboron
Yoshida,Takemoto,Takaki
, p. 6297 - 6300 (2015)
A variety of terminal alkynes are facilely convertible into cis-boryl(stannyl)alkenes with inverse regioselectivity to those of the previous borylstannylation by the copper-catalyzed three-component reaction using a masked diboron. The synthetic utility of the resulting boryl(stannyl)alkenes has been demonstrated by chemoselective coupling reactions. This journal is
A New Preparative Method of Buta-1,3-diene and Hexa-1,5-dien-3-yne by Reduction of Butatriene and Hexapentaene, Respectively, with Zn-ZnCl2-H2O
Kishigami, Satoshi,Tanaka, Koichi,Toda, Fumio
, p. 1877 - 1880 (2007/10/02)
The Zn-ZnCl2-H2O reagent was found to be effective for the reduction of aryl group substituted butatrienes and hexapentaenes to buta-1,3-dienes and hexa-1,5-dien-3-ynes, respectively.