
TY  - JOUR
A1  - Lewis, PH 
A1  - Middleton, S 
A1  - Rosser, MJ 
A1  - Stock, LE 
T1  - Stereochemical Studies. V. Structure of the 'Hydroxymethylene Derivative' Obtained from trans-Decahydronaphthalen-1-one. A Spectroscopic Study
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1979
VL  - 32
IS  - 5
SP  - 1123
EP  - 1129
KW  - 
UR  - https://doi.org/10.1071/CH9791123 
N2  - Formylation of trans-decahydronaphthalen-1-one gives a 'hydroxymethylene derivative' which is, in reality, a complex mixture of stereoisomeric and tautomeric structures; stereochemical integrity at the ring junction is lost during the reaction. The same 'derivative' is obtained on formylation of the isomeric cis-ketone. 
ER  -

