The synthesis of lithium chloroaluminate by melting reaction in dry air is introduced.

According to the strong reducibility of lithium aluminium hydride and asymmetric selectivity of binaphthol,the authors reduce camphor into D-borneol by using D-binaphthol modified lithium aluminium hydride as chiral reagent.

0]nonane (C14H16N2O2)by the reduction of lithium aluminium hydride.

In this method,2,6-Difluorobenzamide used for the raw material,lithium aluminium hydride used for the reducing agent.

A novel reaction of α,β-unsaturated esters and ketones with lithium aluminum hydride in dry tetrahydrofuran solution at 0 ℃ affords, in addition to saturated and unsaturated alcohols, the corresponding 1,3-diols in moderate yield.

A chiral reagent prepared by (1S, 2R) 1 dibutylamino 2 indanol (R*OH) and lithium aluminum hydride was first applied to the asymmetric reduction of acetophenone.

A novel method was developed and carefully studied for the synthesis of polyoxygenated cyclohexene-yl-methanol from shikimic acid by means of esterification with methanol,followed by protection by DMP and TBDMSCl and reduction by mixed THF solution of lithium aluminum hydride and aluminum chloride.

Mutation Screening of L-histidine Producing Strain by UV and LiCl;

Based on UV and LiCl. inducing: the screening of high-producing strains yielding 10-hydroxy-2-decenoic acid;

The effects of LiCl on Tau phosphorylation induced by β-amyloid peptide;