144358-24-7Relevant articles and documents
Structurally simplified squalestatins: A convenient route to a 6,7-unsubstituted derivative
Lester,Gilbin,Inglis,Procopiou,Ross,Watson
, p. 4357 - 4360 (1993)
The squalestatin 1, has been converted into the 6,7-unsubstituted analogue, 3, via inversion of the alcohol at C7, selective removal of the α,β-unsaturated ester at C6 followed by a Corey-Hopkins deoxygenation of the generated 6R,7S-diol.
The Squalestatins: Novel Inhibitors of Squalene Synthase. Enzyme Inhibitory Activities and in Vivo Evaluation of C1-Modified Analogues
Procopiou, Panayiotis A.,Bailey, Esme J.,Bamford, Mark J.,Craven, Andy P.,Dymock, Brian W.,et al.
, p. 3274 - 3281 (2007/10/02)
Squalestatin analogues modified in the C1 side chain were prepared and evaluated for their ability to inhibit rat liver microsomal and Candida squalene synthase (SQS) in vitro.While maintaining the 4,6-dimethyloctenoate or 4,6-dimethyloctanoate ester grou
Chemoselective removal and replacement of the C-4' and C-6 acyl esters of zaragozic acid A
Burk,Berger,Bugianesi,Girotra,Parsons,Ponpipom
, p. 975 - 978 (2007/10/02)
An efficient chemical sequence is described for the modification of the C-4' and C-6 positions of zaragozic acid A. Key reactions include the specific conditions devised for selective removal of either the C-4' acetate or the C-6 acyl chain. The resultant