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Asymmetric cleavage of chiral α,β-ethylenic acetals by organolithium reagents
α,β-Ethylenic chiral acetals react regio- and stereoselectively with organolithium reagents. The obtained enol ether may be hydrolyzed into a chiral β-disubstituted aldehyde. Graphic
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Published in: | Tetrahedron: asymmetry 1996-12, Vol.7 (12), p.3343-3346 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | α,β-Ethylenic chiral acetals react regio- and stereoselectively with organolithium reagents. The obtained enol ether may be hydrolyzed into a chiral β-disubstituted aldehyde.
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ISSN: | 0957-4166 1362-511X |
DOI: | 10.1016/S0957-4166(96)00438-7 |