Explore: Hydroboration

In organic chemistry, hydroboration refers to the addition of a hydrogen-boron bond to certain double and triple bonds involving carbon (C=C, C=N, C=O

Hydroboration–oxidation reaction is a two-step hydration reaction that converts an alkene into an alcohol. The process results in the syn addition of

many chemical transformations in organic chemistry — most importantly, hydroboration and carboboration. Most reactions transfer a nucleophilic boron substituent

ammonia borane as byproduct. The ratio depends on the conditions. In the hydroboration reaction, diborane also reacts readily with alkenes to form trialkylboranes

In chemistry, metal-catalysed hydroboration is a reaction used in organic synthesis. It is one of several examples of homogeneous catalysis. In 1975,

It is a colorless waxy solid that is used in organic synthesis for hydroboration–oxidation reactions. Like most dialkyl boron hydrides, it has a dimeric

Diborane reacts with alkenes to give alkylboranes, a process known as hydroboration: B2H6 + 2 CH2=CHR → 2 BH2(CH2CH2R) B2H6 + 4 CH2=CHR → 2 BH(CH2CH2R)2

organoborane compound. This colourless solid is used in organic chemistry as a hydroboration reagent. The compound exists as a hydride-bridged dimer, which easily

be oxidized to form an alcohol. This two-step reaction is now called hydroboration-oxidation and is a reaction that converts alkenes into anti-Markovnikov

with B-H-B bridges. Diisopinocampheylborane was originally prepared by hydroboration of excess α-pinene with borane, but it is now more commonly generated