Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chun-Hong Yeh"'
Autor:
Chun-Hong Yeh, 葉俊鴻
103
In first part of thesis, synthesis of analogues of ganglioside Hp-s1 varying at central glucosyl moiety is presented. In order to optimize the important role of central glucosyl moiety of ganglioside Hp-s1 in neurology, we have replaced gluc
In first part of thesis, synthesis of analogues of ganglioside Hp-s1 varying at central glucosyl moiety is presented. In order to optimize the important role of central glucosyl moiety of ganglioside Hp-s1 in neurology, we have replaced gluc
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/32973114632437559919
Publikováno v:
Journal of the American Chemical Society. 145:9003-9010
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a549c6c17dd50d9011404dae8dff19f8
https://doi.org/10.1021/jacs.3c00102
https://doi.org/10.1021/jacs.3c00102
Autor:
Shun-Yuan Luo, Hung-Ju Tai, Yu-Hsuan Lih, Satpal Singh Badsara, Shih-An Yang, Hua-Shuan Lin, Chun-Hong Yeh, Ratnnadeep C. Sawant, Chung-Li Huang
Publikováno v:
RSC Adv.. 4:26524-26534
The Wittig reaction of the pyrano-type reducing sugars undergoes an unexpected formation of dienes through the elimination of a benzyloxy group in the presence of t-BuOK. LiHMDS is used rather than t-BuOK to prevent alcohol elimination in the same su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::991c1e3dbd755b37641bfd849e875d42
https://doi.org/10.1039/c4ra03369h
https://doi.org/10.1039/c4ra03369h
Autor:
Yu-Hsuan Lih, Ratnnadeep C. Sawant, Chun-Hong Yeh, Hung-Ju Tai, Chung-Li Huang, Shun-Yuan Luo, Hua-Shuan Lin, Satpal Singh Badsara, Shih-An Yang
Publikováno v:
ChemInform. 46
The Wittig reaction of the pyrano-type reducing sugars undergoes an unexpected formation of dienes through the elimination of a benzyloxy group in the presence of t-BuOK. LiHMDS is used rather than t-BuOK to prevent alcohol elimination in the same su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7846aaf12bef2e7d01f3649c20d285c1
https://doi.org/10.1002/chin.201504218
https://doi.org/10.1002/chin.201504218