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The total synthesis of (-)-cryptocaryol A
L C Dias1, P K Kuroishi, E C de Lucca
1Instituto de Química, Universidade Estadual de Campinas, 13083-970, C.P. 6154, Campinas, SP, Brazil. ldias@iqm.unicamp.br.
Abstract:
A stereoselective total synthesis of (-)-cryptocaryol A (1) is described. Key features of the 17-step route include the use of three boron-mediated aldol reaction-reduction sequences to control all stereocenters and an Ando modification of the Horner-Wadsworth-Emmons olefination that permitted the installation of the Z double bond of the α-pyrone ring.
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