124901-76-4Relevant academic research and scientific papers
Syntheses of two diastereoisomers of panaxytriol, a potent antitumor agent isolated from Panax ginseng
Lu, Wei,Zheng, Guangrong,Gao, Daxin,Cai, Junchao
, p. 7157 - 7168 (2007/10/03)
(3R, 9R, 10R) and (3R, 9S, 10S) diastereoisomers (2 and 3) of panaxytriol (1) were synthesized, and the absolute configuration of panaxytriol was confirmed as (3R, 9R, 10R)-heptadec-1-ene-4,6-diyne-3,9,10- triol.
Synthesis of a new type of antitumour agent panaxytriol: Synthesis of its four diastereomers
Gurjar, Mukund K.,Kumar, V. Sylesh,Rao, B. Venkateswara
, p. 12563 - 12576 (2007/10/03)
Synthesis of four diastereomers of panaxytriol has been described. The basic objective is to create two acetylenic precursors followed by cuprous chloride mediated C-C bond coupling reaction.
First total synthesis of panaxytriol, a potent antitumor agent isolated from Panax ginseng
Lu, Wei,Zheng, Guangrong,Cai, Junchao
, p. 737 - 738 (2007/10/03)
Panaxytriol 1, a potent antitumor agent isolated from Panax ginseng, was first synthesized, and its stereostructure was confirmed to be (3R, 9R, 10R)-heptadec-1-ene-4,6-diyne-3,9,10-triol.
Synthesis and the Absolute Configuration of Panaxacol
Fujimoto, Yasuo,Satoh, Mitsuru,Takeuchi, Naoki,Kirisawa, Makoto
, p. 1619 - 1622 (2007/10/02)
Panaxacol, a polyacetylene isolated from the callus of Panax ginseng, was synthesized from D-(-)-diethyl tartrate.The absolute configuration of panaxacol was determined to be 9R,10R.
