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- W2163071902 abstract "The total synthesis of the polyhalogenated antitumour agent halomon (1) was accomplished with two novel transformations as key steps: a Johnson–Claisen rearrangement of a dichlorinated alkene for the preparation of the tertiary chlorinated C3 and a new rearrangement of bromohydrins for the regiospecific introduction of the bromine and chlorine atoms on C6 and C7, respectively." @default.
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- W2163071902 date "1998-08-17" @default.
- W2163071902 modified "2023-10-03" @default.
- W2163071902 title "Total Synthesis of (±)-Halomon by a Johnson-Claisen Rearrangement" @default.
- W2163071902 doi "https://doi.org/10.1002/(sici)1521-3773(19980817)37:15<2085::aid-anie2085>3.0.co;2-j" @default.
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