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- W2048260380 abstract "The title compound, the most important genotoxic metabolite of benzo[a]pyrene, has been prepared efficiently in a synthesis which capitalized on Jacobsen-type enantioselective epoxidation of 9,10-dihydrobenzo[a]pyrene, cleavage of the epoxide by KOH–Me2SO to give the tetrahydro-trans-7,8-diol, and formation of the dibenzoate from which the contaminating antipode was removed by crystallization." @default.
- W2048260380 created "2016-06-24" @default.
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- W2048260380 date "1995-01-01" @default.
- W2048260380 modified "2023-09-27" @default.
- W2048260380 title "Enantioselective synthesis of the (+)-anti-7,8-dihydrodiol-9,10-epoxide of the potent carcinogen benzo[a]pyrene" @default.
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- W2048260380 doi "https://doi.org/10.1039/c39950001699" @default.
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