125710-44-3Relevant articles and documents
Total Syntheses of Both Enantiomers of Sarcophytols A and T Based on Stereospecific Wittig Rearrangement
Kodama, Mitsuaki,Yoshio, Suzuyo,Yamaguchi, Shinji,Fukuyama, Yoshiyasu,Takayanagi, Hisao,et al.
, p. 8453 - 8456 (1993)
Both enantiomers of sarcophytols A (1) and T (2), cembranolide diterpenes isolated from a soft coral, were syntesized from a common chiral intermediate, obtained by baker's yeast reduction, using a stereospecific Wittig rearrangement as the key step.