Norbornadiene is oxidized by a Pseudomonad to give the diol (2)(35%) while 7-phenylnorbornadiene furnishes 3-norbornadienylcyclohexa-3,5-diene-1,2-diol (10)(41%) on incubation with the same organism; cyclization reactions involving the acetonide (15) have been investigated.
P. J. Geary, R. J. Pryce, S. M. Roberts, G. Ryback and J. A. Winders, J. Chem. Soc., Chem. Commun., 1990, 204 DOI: 10.1039/C39900000204
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