SYNTHESIS OF THE NATURALLY-OCCURRING [3.3.3]PROPELLANE (+ -)-MODHEPHENE FEATURING A PHOTOCYCLOADDITION REDUCTIVE FRAGMENTATION DIQUINANE CONSTRUCTION/

Citation
Ca. Dvorak et Vh. Rawal, SYNTHESIS OF THE NATURALLY-OCCURRING [3.3.3]PROPELLANE (+ -)-MODHEPHENE FEATURING A PHOTOCYCLOADDITION REDUCTIVE FRAGMENTATION DIQUINANE CONSTRUCTION/, Chemical communications, (24), 1997, pp. 2381-2382
Citations number
48
Journal title
ISSN journal
13597345
Issue
24
Year of publication
1997
Pages
2381 - 2382
Database
ISI
SICI code
1359-7345(1997):24<2381:SOTN[(>2.0.ZU;2-C
Abstract
Modhephene has been synthesized in 11 steps and 21% overall yield from cyclopentadiene, by a stereoselective route that features a photocycl oaddition-fragmentation sequence for the construction of the diquinane core.