188050-75-1Relevant academic research and scientific papers
Synthetic study of ciguatoxin. Absolute configuration of the C2 hydroxy group
Oguri, Hiroki,Hishiyama, Shojiro,Sato, Ohki,Oishi, Tohru,Hirama, Masahiro,Murata, Michio,Yasumoto, Takeshi,Harada, Nabuyuki
, p. 3057 - 3072 (2007/10/03)
The absolute stereochemistry of the secondary alcohol of the 1,2-dihydroxybutenyl substituent of ciguatoxin (1) was shown to be S by comparing (he split CD curve of ciguatoxin tetra-p-bromobenzoate (2) with those of di- and tri-p-bromobenzoates of AB ring fragments that were synthesized enaotioselectively.
