Enzyme-catalysed Hydrolysis of 3,5-cis-Diacetoxy-4-trans-benzyloxymethylcyclopentene and the Synthesis of Aristeromycin Precursors
The optically active mono-ester 2 was obtained by enzyme-catalysed hydrolysis of the diester 1 and converted into the azide 8 and the amine 13, synthetic precursors of (+)- and (-)-aristeromycin.
LeGrand, Darren M.,Roberts, Stanley M.
p. 1751 - 1752
(2007/10/02)
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