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- W2952275755 endingPage "3139" @default.
- W2952275755 startingPage "3133" @default.
- W2952275755 abstract "The synthesis of the 1,2,3,4-tetrahydroisoquinoline moiety of tetrazomine was accomplished in 18 steps and in 3% overall yield from commercially available o-anisaldehyde. The reaction sequence utilizes a Sharpless asymmetric dihydroxylation to install the stereocenter and an intramolecular Friedel--Crafts hydroxyalkylation with an N-protected 2-oxo-acetamide to close the heterocyclic ring." @default.
- W2952275755 created "2019-06-27" @default.
- W2952275755 creator A5018024103 @default.
- W2952275755 creator A5033139685 @default.
- W2952275755 date "2001-03-28" @default.
- W2952275755 modified "2023-10-09" @default.
- W2952275755 title "Enantioselective Synthesis of the AB-Ring System of the Antitumor Antibiotic Tetrazomine" @default.
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- W2952275755 doi "https://doi.org/10.1021/jo015512q" @default.
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