Rapid Deprotection of O-Allyoxycarbonyl(alloc) Alcohols by NiCl2•6H2O and NaBH4

Abstract A novel protocol for the deprotection of the O-allyloxycarbonyl(alloc) group by nickel(II) chloride hexahydrate with sodium borohydride in acetone at 0 °C to give the corresponding parent alcohols and phenols in high yields was demonstrated. This method had the advantages of mild reaction conditions and broad substrate scope. The deprotection had also been validated in gram scale, to establish the appropriateness of this protocol.

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Publication Details

Journal
Synlett
Published
2025-09-19
DOI
https://doi.org/10.1055/a-2706-0684
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Rapid Deprotection of O-Allyoxycarbonyl(alloc) Alcohols by NiCl2•6H2O and NaBH4

Jiangmeng Ren, Qian Zeng, Xinxin Yuan, Bu‐Bing Zeng et al.
Synlett
Chemical Synthesis and Reactions
article

Rapid Deprotection of O-Allyoxycarbonyl(alloc) Alcohols by NiCl2•6H2O and NaBH4

Jiangmeng Ren, Qian Zeng, Xinxin Yuan, Bu‐Bing Zeng, Hongmiao Yao, Wen Jin
article en

Abstract

Abstract A novel protocol for the deprotection of the O-allyloxycarbonyl(alloc) group by nickel(II) chloride hexahydrate with sodium borohydride in acetone at 0 °C to give the corresponding parent alcohols and phenols in high yields was demonstrated. This method had the advantages of mild reaction conditions and broad substrate scope. The deprotection had also been validated in gram scale, to establish the appropriateness of this protocol.

SynlettVol. 37(02)
East China University of Science and Technology (CN), Zhejiang Hisun Pharmaceutical (China) (CN), Zhejiang Pharmaceutical College (CN), Zhejiang Medicine (China) (CN)
Openalex Percentile: Top 81%
Chemical Synthesis and Reactions
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