100536-95-6Relevant articles and documents
One-Pot Conversions of (Silylmethyl)cyclopropanes to Homoallylic Alcohols and 1,4-Diols Based on Haloborane-Induced Ring Opening
Ryu, Ilhyong,Hirai, Akira,Suzuki, Haruhisa,Sonoda, Noboru,Murai, Shinji
, p. 1409 - 1410 (1990)
The reactions of (silylmethyl)cyclopropanes with haloboranes, such as BBr3 and BHBr2, result in desilylative ring opening to give homoallylboranes and boracyclopentanes, respectively.Coupled with subsequent oxidation procedure, these reactions provide ready access to homoallylic alcohols and 1,4-diols.
Catalytic enantioselective ethylalumination of terminal alkenes: Substrate effects and absolute configuration assignment
Parfenova, Lyudmila V.,Kovyazin, Pavel V.,Tyumkina, Tatyana V.,Makrushina, Alyona V.,Khalilov, Leonard M.,Dzhemilev, Usein M.
, p. 124 - 135 (2015/02/19)
The chemo- and enantioselectivity of the reaction of alkenes with AlEt3 catalyzed by bis(1-neomenthylindenyl)zirconium dichloride has been studied. The reaction with linear alkenes in a chlorinated solvent (CH2Cl2) gives m