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Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway†
Daniel. M. Evans,Peter N. Horton,Michael B. Hursthouse,Patrick. J. Murphy
RSC Advances Pub Date : 04/28/2014 00:00:00 , DOI:10.1039/C4RA03031A
Abstract

Two tricyclic guanidine model compounds 28 and 29 have been prepared in 12 steps from 1,5-pentanediol using a biomimetic synthetic approach. The pivotal reaction in the sequence is a tethered Biginelli condensation between 21/22 and β-keto esters 23 and 24.

Graphical abstract: Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway
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