期刊
ORGANIC LETTERS
卷 3, 期 18, 页码 2935-2938出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol016490x
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资金
- NIGMS NIH HHS [GM35956] Funding Source: Medline
[GRAPHICS] The intramolecular, stereoselective addition of 1-vinylcyclopropanols to tethered aldehydes has been achieved under mild conditions. Thus, sequential application of the titanium-mediated cyclopropanation of alpha,beta -unsaturated esters and the electrophilic cyclization of the aldehyde-tethered cyclopropanol products provides the facile formation of carbocyclic rings.
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