
TY  - JOUR
A1  - Brecknell, DJ 
A1  - Carman, RM 
A1  - Robinson, WT 
A1  - Schumann, RC 
T1  - A Facile Synthesis of a 2,2,3,3-Tetrasubstituted Tetrahydropyran
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1991
VL  - 44
IS  - 8
SP  - 1115
EP  - 1123
KW  - 
UR  - https://doi.org/10.1071/CH9911115 
N2  - An unusually facile acid- catalysed condensation has been observed between acetone and the unsaturated diol (3), producing a mixture of isomeric bicyclic tetrahydropyrans (6) and (8), with the formation of a new fully substituted carbon-carbon single bond. The structures were determined by n.m.r. and that of the major product (6) was confirmed by X-ray crystallography. 
ER  -

