Journal of the Chemical Society. Chemical communications p. 628 - 629 (1993)
Update date:2022-08-11
Topics:
Ouchi, Akihiko
Adam, Waldemar
The formation of acenaphthene 4 by laser-jet photolysis of 1,8-bis(phenoxymethyl)- (1a), 1,8-bis(phenylthiomethyl)- (1b) and 1,8-bis(phenylselenomethyl)-naphthalene (1c) strongly depends on the hetroatom of the leaving group; the increasing order of naphthalene consumption was 1c ca. 1b > 1a, whereas that for the formation of 4 was 1c > 1a > 1b.
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