55976-13-1Relevant articles and documents
Novel type of carbozirconation reaction of alkynes
Suzuki, Noriyuki,Kondakov, Denis Y.,Kageyama, Motohiro,Kotora, Martin,Hara, Ryuichiro,Takahashi, Tamotsu
, p. 4519 - 4540 (1995)
Novel type of carbozirconation reaction of alkynes is reported. Treatment of zirconocenealkyne complexes, zirconacyclopentenes, or zirconacyclopentadienes with allylic compounds gave allylzirconation products of alkynes. Carbozirconation of alkynes with zirconacyclopentenes or zirconacyclopentadienes involved β,β'-C-C bond cleavage reaction of zirconacycles. Reactions of zirconacyclopentenes with homoallyl bromides afforded allylcyclopropane derivatives as carbozirconation products.
Engaging Alkenyl Halides with Alkylsilicates via Photoredox Dual Catalysis
Patel, Niki R.,Kelly, Christopher B.,Jouffroy, Matthieu,Molander, Gary A.
supporting information, p. 764 - 767 (2016/03/01)
Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for the construction of Csp3-Csp2 bonds through the transfer of alkyl radicals under very mild reaction conditions. A general procedure for the cross-coupling of primary and secondary (bis-catecholato)alkylsilicates with alkenyl halides is presented. The developed method allows not only alkenyl bromides and iodides but also previously underexplored alkenyl chlorides to be employed. (Chemical Equation Presented).
Reduction of acetylenic compounds to (E)-olefins by alkali metals - An investigation of the scope
Brandsma, Lambert,Nieuwenhuizen, Willem F.,Zwikker, Jan W.,Maeeorg, Uno
, p. 775 - 779 (2007/10/03)
Efficient procedures have been developed for the stereospecific reduction by alkali metals of disubstituted acetylenes with long carbon chains. Acetylenes containing two or more (isolated) triple bonds are reduced considerably more easily than are monoyne