Stereoselective synthesis of β-branched phenylalanine derivatives via chelate-claisen rearrangement
Ester enolate Claisen rearrangement of chelated N-protected chiral amino acid cinnamyl esters results in the formation of substituted phenylalanine derivatives with unsaturated side chains in good yields and with a high degree of chirality transfer. Georg
Quirin, Christian,Kazmaier, Uli
experimental part
p. 1725 - 1731
(2009/12/22)
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