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January 1, 1999Chemical Communications

Total synthesis of (S)-espicufolin and absolute structure determinaton of espicufolin

Hidemitsu Uno Katsuji Sakamoto Erina Honda Noboru Ono

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Abstract

(S)-Espicufolin was synthesized from 1,4-dimethoxybenzene in 16 steps via an intramolecular acyl-transfer reaction as the key step; the absolute stereochemistry at the 14-position of natural espicufolin was determined to be R.

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Uno et al. (1999) studied this question.

synapsesocial.com/papers/6a990f047a0bd180b0e11ae8 https://doi.org/10.1039/a901602c

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