TY - JOUR
T1 - A brief synthesis of the Aplasmomycin tetrahydrofuran
AU - Bew, Sean P.
AU - Knight, David W.
AU - Middleton, Robert J.
PY - 2000/6/8
Y1 - 2000/6/8
N2 - A highly stereoselective iodocyclisation of the 3-alkene-1,2-diol 9, derived from asymmetric dihydroxylation of the dienyl benzoate 8, gives the β-iodotetrahydrofuran 10 and thence the Aplasmomycin precursor 13, following deiodination and Mitsunobu inversion. (C) 2000 Elsevier Science Ltd.
AB - A highly stereoselective iodocyclisation of the 3-alkene-1,2-diol 9, derived from asymmetric dihydroxylation of the dienyl benzoate 8, gives the β-iodotetrahydrofuran 10 and thence the Aplasmomycin precursor 13, following deiodination and Mitsunobu inversion. (C) 2000 Elsevier Science Ltd.
UR - http://www.scopus.com/inward/record.url?scp=0034622047&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)00614-6
DO - 10.1016/S0040-4039(00)00614-6
M3 - Article
AN - SCOPUS:0034622047
SN - 0040-4039
VL - 41
SP - 4453
EP - 4456
JO - Tetrahedron Letters
JF - Tetrahedron Letters
IS - 22
ER -