696574-71-7Relevant articles and documents
Synthesis of (+)-zeylenone from shikimic acid
Liu, An,Liu, Zhan Zhu,Zou, Zhong Mei,Chen, Shi Zhi,Xu, Li Zhen,Yang, Shi Lin
, p. 3689 - 3694 (2004)
Starting from shikimic acid, the total synthesis of zeylenone was studied. The product was proved to be the (+)antipode of zeylenone through analysis and comparison of their respective spectra (including NMR, MS, IR and CD) and optical data. The absolute
A Lemieux-Johnson oxidation of shikimic acid derivatives: Facile entry to small library of protected (2S,3S,4R)-2,3,4,7-tetrahydroxy-6-oxoheptanals
Psotka, Miroslav,Martinková, Miroslava,Gonda, Jozef
, p. 709 - 719 (2017/03/29)
The Lemieux-Johnson oxidation was employed for the cleavage of the carbon-carbon double bond of shikimic acid derivatives. Through this procedure, a series of the sixteen novel (2S,3S,4R)-2,3,4,7-tetrahydroxy-6-oxoheptanals bearing three contiguous stereo