Lithium aluminum hydride

Abstract

This article has no abstract. Keywords: reviews; determination; history; technique of handling; techniques of reduction; destruction of excess reagent; reduction of aldehydes and ketones; carboxylic acids and derivatives; epoxides; halides and tosylates; amides; aldehyde synthesis; reduction of allylic and propargylic alcohols; α,β-unsaturated esters; aziridine syntheses; aziridine syntheses; homogeneous hydrogenation catalyst; reduction of allylic alcohols; reduction of aryl halides; intramolecular cyclization; reductive dehalogenation of alkyl halides; stereoselective reduction; 3,3-disubstituted 3H-indoles; reductive desulfurization; reductive dehalogenation; reductive aromatization of 4,4-dimethyl steroids; cyclobutenones; conjugated bisallenes; α-allenic alcohols; β-allenic alcohols; contraction of five-membered cyclic sulfones to cyclobutenes; reductive alkylation of amides; asymmetric reductions; allylic rearrangement; tetramethylhydrazine; reductive rearrangement of 2-hexenepyranosides; reduction of a hindered nitrobenzene; conjugated dienes; N-alkylation of sec-amines; examples; reduction of quinones to dihydrodiols; reduction of 1,2-epoxides; reduction of an α,β-unsaturated epoxide; vinyl sulfides; retrosulfolene reaction; contraction of sulfolanes to cyclobutenes; primary alkyl amines; hydroalumination; terminal acetylenes; terminal allenes; reduction of a furanose ditosylate; reduction of acetylenic primary alcohols to (E)-alkenols; (E)-2-alkenenitriles; stereospecific reduction of an enone; reductive grob-like fragmentation; hydroalumination of alkenes; hydroalumination of 1-chloro-1-alkynes; reduction of ω -alkynols to (E)-alkenols; influence of solvents; γ-amino alcohols; reduction of isoxazolines; 3-amino alcohols; allenic alcohols; allylic 1,2-diols; γ-lactone annelation; diastereoselective reduction of chiral β-keto sulfoxides; hydrodehalogenation; syn-1,3-amino alcohols; α-alkenylcarbinols; denitration of α-nitro ketones; regio- and stereospecific reduction of α-oxoketene thioacetals; reduction of aryl and alkyl halides; reductions in benzene or hexane; anti-selective reduction of; reduction of α-methyl-β-hydroxy ketones; reduction of amino acids to amino alcohols; selective desilylation; reduction of 2-arylidenecycloalkanones; heterocycle transformation; dephosphonylation; allylic alcohols; reductive esterification; cleavage of tbs ethers; propargylic mercaptan; reduction of amides; α-ketols; hydrogenation of allylic alcohols; 2-nitroalkanols; γ-amino alcohols; reductive desulfonylation; reduction of alkynols; deoxygenation; isoxazoline cleavage; debromination; conjugate dienes; selenocyclobutenes; piperidines; allylic reduction; organoindium reagents; N-Functionalization; indium(III) bromide; skeletal reorganization; iodosuccinimide, NIS