
TY  - JOUR
A1  - Hamon, DPG 
A1  - Taylor, GF 
T1  - A synthesis of tetracyclo[5,3,1,1<sup>2,6</sup>,0<sup>4,9</sup>]dodecane (iceane)
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1976
VL  - 29
IS  - 8
SP  - 1721
EP  - 1734
KW  - 
UR  - https://doi.org/10.1071/CH9761721 
N2  - A description is given of the chemistry which led to the synthesis of the title compound (1). Key intermediate compounds in this synthetic route were tricyclo[5,3,1,04,9]undec-5-en-2-one (13), tricyclo[5,3,1,04,9]undec-2-en-endo-6-ylmethanol (36) and the exo and endo isomers of chloroiceane (42) and (44). Compound (42) must have a chlorine atom in the prow position of one of the three rings in boat configurations. 
ER  -

