Diisobutylaluminum Hydride, (DIBAL‐H)

Abstract

This article has no abstract. Keywords: preparation; reduction of acetylenes; reduction of quinoline; reduction of a γ-lactone; isomerization of an epoxide; ArCN ArCHO; other reductions; cleavage of α,β-unsaturated ethers; reduction of an α,β-unsaturated γ-lactone to a furane; other reductions; reduction of an α,β-unsaturated γ-lactone to a furane; hydroalumination of alkynes; selective reduction of 2-ene-1,4-diones and 2-ene-1-ones; trans,trans-1,3-Dienes; cyclopropanes; trans-allylic alcohols; conjugate reduction of α,β-unsaturated epoxides; selective reduction; trans-γ,Δ-unsaturated ketones; selective reduction of diethyl homophthalate; reduction of sulfones to sulfides; review; trans-1,4-dienes; trans-3-alkenols; β-hydroxyalkylsilanes; spirobenzylisoquinolines; reduction of α,β-unsaturated γ-lactones to furanes; stereoselective reduction of tropinone; 3,5-dioxocyclopentenes (2); α-amino aldehydes; β-hydroxyalkenes; β,γ-unsaturated carbonyl compounds; trans-Alkenes; trans-Allyl ethyl ethers; intramolecular cyclizations of polyenes; reduction of allylic esters; stereoselective synthesis of a homoallylic alcohol; aldol cyclization; reduction of propargylamines; reduction of allenes; 1,4-reduction of α-oxoketene dithioacetals; pictet-Spengler isoquinoline synthesis; α-alkyl-substituted aldehydes; monoalkylation of polyamines; 1-halo-1-alkenes; reduction of isoflavenones; selective reduction of α,α-dihalo ketones; ate complex with n-buli (2); reduction of oximes; reaction with chiral acetals; Δ1-pyrrolines; Δ1-piperideines; diastereoselective reduction of chiral β-keto sulfoxides; hydroalumination of ω-t-butoxyalkynes; diastereoselective reduction of chiral β-keto sulfoxides; α-trimethylsiloxy aldehydes; regioselective reduction of terminal epoxides; asymmetric synthesis of 1,3-diols; regioselective reduction of 2,3-epoxy alcohols; reductive cleavage of t-butyldimethylsilyl ethers; monosilyl acetals and amines; opening of oxabicycles; special preparations; cyclic ethers from spiroacetals; α-acetoxy ethers; amines from amides; hydroalumination; removal of bornane-10,2-sultam auxiliary; deallylation; elimination; carbonyl reduction; modified Baylis–Hillman reaction; activation of chalcogens; reductive chloroallylation and thioallylation; reduction; aminolysis; reduction; rearrangement; hydroalkylation; reductive cleavage; Baylis-Hillman reaction; cycloisomerization; dibutylboron alkoxides and dicarboxylates; 4,5-Dichlorophthaloyl peroxide; dimethyldioxirane, DMDO