期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 73, 期 2, 页码 752-755出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo7021923
关键词
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资金
- NIGMS NIH HHS [P50 GM-069663] Funding Source: Medline
[GRAPHICS] Employing TMSOTf as an easily available reagent, we have developed a mild and efficient method for the deprotection of both terminal and internal NO-acetonide functionalities. Various regularly used protecting groups and common organic functional moieties were found to be unaffected by the described reaction conditions. In a few representative examples, the present method was also extended to deprotect acetonides obtained from 1,2-, and 1,3-terminal diols. The acetonide deprotection protocol described herein is expected to be a useful addition to the presently available methods for performing the above transformation.
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