Contrasting photosolvolytic reactivities of 9-fluorenol vs. 5-suberenol derivatives. Enhanced rate of formation of cyclically conjugated four. pi. carbocations in the …
P Wan, E Krogh
Index: Wan, Peter; Krogh, Erik Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4887 - 4895
Full Text: HTML
Citation Number: 63
Abstract
Abstract: The photosolvolysis of 9-fluorenol (1) and several of its derivatives, as well as related systems, has been studied in aqueous methanol and acetonitrile solutions. The primary aim of this study was to examine the effect of the internal cyclic array (ICA) of these compounds in promoting photosolvolysis with respect to the number of P electrons available in the ICA. It was observed that 9-fluorenol derivatives photosolvolyze much more ...
Related Articles:
[Valenta, Vladimir; Hulinska, Hana; Holubek, Jiri; Dlabac, Antonin; Metys, Jan; et al. Collection of Czechoslovak Chemical Communications, 1988 , vol. 53, # 4 p. 860 - 869]
[Canadian Journal of Chemistry, , vol. 47, p. 4327 - 4333]
[Canadian Journal of Chemistry, , vol. 47, p. 4327 - 4333]
[Journal of Medicinal Chemistry, , vol. 37, # 6 p. 804 - 810]
[Canadian Journal of Chemistry, , vol. 47, p. 4327 - 4333]