ol050713s_si_001.pdf (1.62 MB)
Total Synthesis of Hyacinthacine A1 and 3-epi-Hyacinthacine A1
journal contribution
posted on 2005-06-23, 00:00 authored by Laurent Chabaud, Yannick Landais, Philippe RenaudTotal synthesis of hyacinthacine A1 and its epimer at C3 is described. The synthesis includes a stereocontrolled carboazidation of a chiral
allylsilane as a key step. C−Si bond oxidation and reduction of the azide, with ring-closure, complete the total synthesis, which establishes
the absolute configuration of 3.