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- W2054696593 abstract "A conformationally constrained 10-membered cyclic diamide was designed and synthesized. Conformational analysis suggested that the 9-membered ring formation was preferred to the direct formation of 10-membered ring. On the basis of the prediction, lactonization of 9-membered lactone, followed by intramolecular ester–amide transformation afforded the desired 10-membered cyclic diamide." @default.
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- W2054696593 date "2002-04-01" @default.
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- W2054696593 title "Synthesis of a tetrabenzyl-substituted 10-membered cyclic diamide" @default.
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- W2054696593 doi "https://doi.org/10.1016/s0040-4020(02)00204-1" @default.
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