Total Synthesis of Hydroxylated Analogues of Ganglioside Hp-s1 Varying in Stereochemistry at C-3 and C-5 Positions
碩士 === 國立中興大學 === 化學系所 === 102 === Ganglioside Hp-s1, which was first isolated from Diadema setosum, displays good neuritogenic activity. Syntheses of hydroxylated analogues of Hp-s1 with varied stereochemistry based on glucose, galactose, mannose and talose are described. The essential stereochemis...
Main Authors: | Yu-Hsuan Lih, 酈又瑄 |
---|---|
Other Authors: | 羅順原 |
Format: | Others |
Language: | zh-TW |
Published: |
2014
|
Online Access: | http://ndltd.ncl.edu.tw/handle/71605925275071361916 |
Similar Items
-
Total Synthesis of Ganglioside Hp-s1
by: Wan-Shin Chen, et al.
Published: (2014) -
Synthesis of Ganglioside Hp-s1 and Its Phytosphingosine Modified Analogues
by: Ying-Ju Liao, et al.
Published: (2014) -
Control of the stereochemistry of C14 hydroxyl during the total synthesis of withanolide E and physachenolide C
by: Anees, Muhammad, et al.
Published: (2018) -
(1) Preparation of Derivative of Sphingosine (2) Concise Synthesis of Ganglioside Hp-s1 Analogue
by: Pin-Yu Jiang, et al.
Published: (2016) -
The stereochemistry of enzymic hydroxylation
by: Suckling, K. E.
Published: (1971)