1106402-00-9Relevant academic research and scientific papers
Synthesis and configuration of the phenolic nonadecanediol isolated from the resinous exudates of heliotropium sinuatum
Chen, Chao-Yuan,Zhang, Shao-Min,Wu, Yikang,Gao, Po
, p. 348 - 355 (2013/02/26)
The (3S,5R) and (3R,5R) isomers of the title compound were synthesized from enantiopure epoxide chiral building blocks readily accessible from D-gluconolactone. The former (a syn-1,3-diol) gave 1H and 13C NMR spectroscopic data and optical rotation in good agreement with those reported for the natural product, whereas distinct differences were found with the data for the latter (an anti-1,3-diol). These results unambiguously showed that the absolute configuration of the natural product must be (3S,5R).
Facile access to some chiral building blocks. Synthesis of verbalactone and?exophilin A
Wu, Jian-Zhong,Gao, Jian,Ren, Guo-Bao,Zhen, Zhi-Bin,Zhang, Yihua,Wu, Yikang
experimental part, p. 289 - 299 (2009/04/06)
d-Glucono-1,5-lactone, an inexpensive carbohydrate, was elaborated into chiral building blocks readily applicable in synthesis via practical routes without involving any expensive reagents or tedious operations. Application of such chiral building blocks
