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- W2060271569 abstract "Four bis-unsaturated N-benzyl amides of the type where (C2) and (C2)' are variously trans-CHCH and CC groups, were synthesized and refluxed in acetic anhydride. Three of them cyclized to form N-benzylcyclolignan lactams by intramolecular Diels-Alder processes. In one case [(C2) CC, (C2)' trans-CHCH] the (C2) unit functioned as the dienophilic moiety." @default.
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- W2060271569 date "1972-12-01" @default.
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- W2060271569 title "Intramolecular diels-alder reactions. IX. Syntheses of<i>N</i>-benzylcyclolignan lactams" @default.
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- W2060271569 doi "https://doi.org/10.1002/jhet.5570090604" @default.
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