Fluoranthene: Synthesis and mutagenicity of four diol epoxides

Rastetter, WH; Nachbar, RB; Russo-Rodriguez, S; Wattley, RV; Thilly, WG; Andon, BM; Jorgensen, WL; Ibrahim, M

HERO ID

628510

Reference Type

Journal Article

Year

1982

HERO ID 628510
In Press No
Year 1982
Title Fluoranthene: Synthesis and mutagenicity of four diol epoxides
Authors Rastetter, WH; Nachbar, RB; Russo-Rodriguez, S; Wattley, RV; Thilly, WG; Andon, BM; Jorgensen, WL; Ibrahim, M
Journal Journal of Organic Chemistry
Volume 47
Issue 25
Page Numbers 4873-4878
Abstract The syntheses of diol epoxides 4a,b and 5a,b of the mutagenic hydrocarbon fluoranthene (1) are described. Standard methodology is applied to the synthesis of targets 4a,b but fails for the synthesis of 5a,b. The latter two diol epoxides can be assembled by a route utilizing stereoselective, directed epoxidations. Simple molecular orbital calculations have been used to predict the reactivity of the diol epoxides in their opening to triol carbocations. Diol epoxides 4a,b are predicted to be substantially more reactive than isomers 5a,b. The more reactive pair, 4a,b, may yield carbocations capable of alkylating cellular genetic material. This prediction is borne out in terms of the relative mutagenicity of the diol epoxides in a bacterial screen.
Doi 10.1021/jo00146a011
Url http://pubs.acs.org/doi/abs/10.1021/jo00146a011
Is Certified Translation No
Dupe Override 628510
Comments Journal: J ORG CHEM 47 ISSN:
Is Public Yes
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