Stereoselective synthesis of the C(1)-C(12) fragments of tedanolides - Application of a syn-selective tin(II)-mediated aldol reaction and a convertible methoxybenzyl protecting group
K. Matsui et al., Stereoselective synthesis of the C(1)-C(12) fragments of tedanolides - Application of a syn-selective tin(II)-mediated aldol reaction and a convertible methoxybenzyl protecting group, EUR J ORG C, (19), 2001, pp. 3615-3624
Stereoselective synthesis of two C(1)-C(12) fragments, 3 and 4, of antitumo
r agents tedanolide (1) and 13-deoxytedanolide (2) was achieved by means of
several regio- and/or stereoselective reactions. Ethyl ketone 14 was synth
esized from methyl (S)-3-hydroxy-2-methylpropionate (16a) by way of a Weinr
eb amide. A highly syn-selective tin(II)-mediated aldol reaction between 14
and aldehyde 15, prepared from (R)-propionate 16b, proceeded smoothly, and
subsequent reduction gave diol 13, which was transformed into 3, incorpora
ting a C(3),C(5)-MP acetal moiety, by taking advantage of convertible MPM p
rotecting groups. Another fragment, 4, with C(3)-O-methyl and C(5)-O-MPM gr
oups, was also synthesized. A crucial step was the selective transformation
of C(2),C(3)-diol 21 into C(2)-O-TBS, C(3)-O-Me compound 22.