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• W2165313973 abstract "A new class of aminocyclitol derivatives with the bicyclo[4.2.0]octane skeleton was synthesized starting from cyclooctatetraene. Photooxygenation of trans -7,8-diacetoxy- and cis -7,8-dichlorobicyclo[4.2.0]octa-2,4-diene afforded the bicyclic endoperoxides. Reduction of the latter with thiourea followed by a Pd(0) catalyzed ionization/cyclization reaction gave the corresponding oxazolidinone derivatives. Oxidation of the double bond with KMnO 4 or OsO 4 followed by acetylation gave the acetate derivatives, the exact configuration of which was determined by spectroscopic methods. Hydrolysis of the oxazolidinone rings and removal of the acetate groups furnished the desired aminocyclitols." @default.
• W2165313973 created "2016-06-24" @default.
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• W2165313973 creator A5020114981 @default.
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• W2165313973 date "2010-02-15" @default.
• W2165313973 modified "2023-09-26" @default.
• W2165313973 title "Synthesis of a new class of aminocyclitol analogues with the conduramine D-2 configuration" @default.
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• W2165313973 doi "https://doi.org/10.3762/bjoc.6.15" @default.
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