Journal of the Chemical Society. Chemical communications p. 204 - 205 (1990)
Update date:2022-07-29
Topics:
Geary, Philip J.
Pryce, Robert J.
Roberts, Stanley M.
Ryback, George
Winders, John A.
Norbornadiene is oxidized by a Pseudomonad to give the diol (2) (35percent) while 7-phenylnorbornadiene furnishes 3-norbornadienylcyclohexa-3,5-diene-1,2-diol (10) (41percent) on incubation with the same organism; cyclization reactions involving the acetonide (15) have been investigated.
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