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- W2952911247 abstract "The chemistry of a conformationally locked tricyclo[9.3.1.03,8]pentadecane skeleton, prepared by an atropselective type 2 intramolecular Diels-Alder reaction, is examined. In many cases, the conformation of the tricycle controls the facial selectivity of the addition of nucleophilic and electrophilic reagents to this ring system." @default.
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- W2952911247 date "1992-08-01" @default.
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- W2952911247 title "Stereoselective elaboration of the tricyclo[9.3.1.03,8]pentadecane ring system. Atropisomeric control of stereochemistry" @default.
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- W2952911247 doi "https://doi.org/10.1016/s0040-4039(00)61261-3" @default.
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