TORSIONAL ANGLE DECOMPRESSION IS NOT THE SOURCE OF FACIAL SELECTIVITY IN DIELS-ALDER CYCLOADDITIONS INVOLVING CYCLIC DIENES FUSED TO BICYCLIC FRAMEWORKS - THE CASE-STUDY OF 1,2,3,4,6,7-HEXAHYDRO-1,4-METHANONAPHTHALENE
被引:13
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作者:
HICKEY, ER
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OHIO STATE UNIV,EVANS CHEM LABS,COLUMBUS,OH 43210OHIO STATE UNIV,EVANS CHEM LABS,COLUMBUS,OH 43210
HICKEY, ER
[1
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PAQUETTE, LA
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h-index: 0
机构:
OHIO STATE UNIV,EVANS CHEM LABS,COLUMBUS,OH 43210OHIO STATE UNIV,EVANS CHEM LABS,COLUMBUS,OH 43210
PAQUETTE, LA
[1
]
机构:
[1] OHIO STATE UNIV,EVANS CHEM LABS,COLUMBUS,OH 43210
Hydrocarbon 3 has been synthesized and shown to enter into Diels-Alder cycloaddition preferentially from the top face. This behavior, and that of 2, cannot be accounted for in terms of torsional strain minimization.