1054623-05-0Relevant articles and documents
Determination of the absolute configuration of the cytotoxic natural product pericosine D
Usami, Yoshihide,Mizuki, Koji,Ichikawa, Hayato,Arimoto, Masao
, p. 1460 - 1463 (2008)
The synthesis of two diastereomers of pericosine A from (-)-quinic acid was achieved, thus enabling the confirmation of the relative configuration and elucidation of the absolute stereochemistry of cytotoxic natural product pericosine D assigned as methyl (3R,4R,5S,6R)-6-chloro-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate.