1988
DOI: 10.1055/s-1988-27782
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Reduction of Some Functional Groups with Zirconium Tetrachloride/Sodium Borohydride

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Cited by 73 publications
(21 citation statements)
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“…Although the combination system of NaBH 4 and ZrCl 4 has been reported for reduction of oximes 12 or o-alkyl oxime ethers;…”
Section: Resultsmentioning
confidence: 99%
“…Although the combination system of NaBH 4 and ZrCl 4 has been reported for reduction of oximes 12 or o-alkyl oxime ethers;…”
Section: Resultsmentioning
confidence: 99%
“…Though there are several procedures known, more efficient and convenient protocols are continously being explored. The reduction of carboxylic acids was achieved by a variety of metal hydride based reducing agents such as LiAlH 4 reported in the literature. BOP reagent was used to activate carboxylic group prior to NaBH 4 treatment.…”
Section: T R a C Tmentioning
confidence: 99%
“…The reduction of C=O double bonds, C=N double bonds and C N triple bonds in THF at room temperature has been achieved using ZrCl 4 /NaBH 4 (Scheme 16) [58]. The procedure works well for aldehydes, ketones, carboxylic acids, carboxylic esters, acyl chlorides, carboxamides, oximes and nitriles.…”
Section: Reduction Of C=o Double Bonds C=n Double Bonds and C N Tripmentioning
confidence: 99%