TY - JOUR
T1 - Diastereoselective and highly efficient radical approach to (1S,6R) and (1R,6S)-2,2,6-trimethyl-3-oxabicyclo[4.2.0]octadecane, key intermediates in the synthesis of (+) and (-)-grandisol
AU - Alibés, Ramón
AU - Bourdelande, José L.
AU - Font, Josep
PY - 1994/4/18
Y1 - 1994/4/18
N2 - The pure enantiomers (1S,6R) and (1R,6S)-2,2,6-trimethyl-3-oxabicyclo[4.2.0]octadecane, key intermediates in the synthesis of (+) and (-)-grandisol are prepared by a highly efficient radical deoxygenation under mild conditions of secondary hydroxyl groups. © 1994.
AB - The pure enantiomers (1S,6R) and (1R,6S)-2,2,6-trimethyl-3-oxabicyclo[4.2.0]octadecane, key intermediates in the synthesis of (+) and (-)-grandisol are prepared by a highly efficient radical deoxygenation under mild conditions of secondary hydroxyl groups. © 1994.
U2 - 10.1016/S0040-4039(00)77178-4
DO - 10.1016/S0040-4039(00)77178-4
M3 - Article
VL - 35
SP - 2587
EP - 2588
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 16
ER -