864064-32-4Relevant academic research and scientific papers
Stereoselective syntheses of diastereomers of antitumor natural product pericosine A from (-)-quinic acid
Usami, Yoshihide,Ueda, Yasuko
, p. 3219 - 3225 (2007)
The stereoselective syntheses of diastereomers of antitumor natural pericosine A from (-)-quinic acid were achieved. One of the diastereomers, methyl (3R,4S,5S,6R)-6-chloro-3,4,5-trihydroxycyclohex-1-enecarboxylate, possesses the reported structure of per
Synthetic study toward antitumour natural product pericosine A
Usami, Yoshihide,Ueda, Yasuko
, p. 1062 - 1063 (2007/10/03)
The stereoselective total synthesis of methyl (3R,4S,5S,6R)-6-chloro-3,4,5- trihydroxy-1-cyclohex-1-enecarboxylate (1), which had been reported as the antitumour marine natural product pericosine A, from (-)-quinic acid was achieved. From the total synthesis, it was confirmed that the reported stereostructure of pericosine A was incorrect because the spectroscopic data of the synthetic product were not identical with those of the natural compound. Copyright
