A diastereoselective route to substituted β-amino acids using enolate Claisen rearrangements
- 1 January 1989
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 23,p. 1812-1814
- https://doi.org/10.1039/c39890001812
Abstract
Ireland-type enolate Claisen rearrangements of esters derived from allylic alcohols and N-alkoxycarbonyl-β-alanines lead to good yields of α-allyl-β-amino acids with generally high stereoselectivities.Keywords
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