2003
DOI: 10.1002/chin.200322048
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Oxidation of Benzylic Alcohols and Ethers to Carbonyl Derivatives by Nitric Acid in Dichloromethane.

Abstract: For Abstract see ChemInform Abstract in Full Text.

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Cited by 3 publications
(3 citation statements)
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“…Because the oxidation of benzyl alcohols and benzyl methyl ethers to the corresponding aldehydes is common, 16 18 we envisioned that benzyl alcohols and benzyl methyl ethers might be used directly instead of aldehydes ( Scheme 1 D).…”
Section: Introductionmentioning
confidence: 99%
“…Because the oxidation of benzyl alcohols and benzyl methyl ethers to the corresponding aldehydes is common, 16 18 we envisioned that benzyl alcohols and benzyl methyl ethers might be used directly instead of aldehydes ( Scheme 1 D).…”
Section: Introductionmentioning
confidence: 99%
“…organomagnesium reagents to 2,4,6-trichlorophenyl isocyanide then following reactions leading to an efficient synthesis of benzil compounds [24]. Facile oxidation of benzylic alcohols and benzoin to give benzil compounds with various oxidation reagents had been reported [24][25][26][27][28][29][30][31][32].…”
mentioning
confidence: 99%
“…For example, electrophilic aromatic nitration of benzylic chlorides uses harsh conditions and often leads to a regioisomeric mixture of products. 6,7 In this context, we have proposed a new synthetic strategy leading to selectively substituted o-nitrobenzyl chlorides by nucleophilic aromatic substitution of hydrogen of nitrobenzenes via the vicarious nucleophilic substitution (VNS) process. 8,9 Direct nucleophilic aromatic chloromethylation has not been achieved, but there are several reports in the literature of VNS leading to nitrosubstituted benzylic products.…”
mentioning
confidence: 99%