An article Total Synthesis of Sialyl Inositol Phosphosphingolipids CJP-2, CJP-3, and CJP-4 Isolated from Feather Star Comanthus japonica WOS:000471212100039 published article about 1ST TOTAL-SYNTHESIS; STEREOSELECTIVE-SYNTHESIS; NEURITOGENIC ACTIVITY; GANGLIOSIDE; ACID; FACILE; CONSTITUENTS; DERIVATIVES; CRINOIDEA; GLYCAN in [Tanaka, Hide-Nori; Ishida, Hideharu; Ando, Hiromune] Gifu Univ, Ctr Highly Adv Integrat Nano & Life Sci G CHAIN, Gifu 5011193, Japan; [Goto, Kenta; Tamai, Hideki; Takeda, Yoh; Mizuno, Takashi; Imamura, Akihiro; Ishida, Hideharu; Kiso, Makoto] Gifu Univ, Fac Appl Biol Sci, Dept Appl Bioorgan Chem, Gifu 5011193, Japan; [Kiso, Makoto; Ando, Hiromune] Kyoto Univ, Inst Integrated Cell Mat Sci WPI iCeMS, Kyoto 6068501, Japan in 2019, Cited 52. Product Details of 93-97-0. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0
The first total synthesis of three echinodermatous sialyl inositol phosphosphingolipids, which exhibit unusual neuritogenic activity in the absence of nerve growth factor, are reported. Highlights of the syntheses include 9-O-methylation on sialic acid, inter-residual amide bond formation between sialic acid residues, and highly stereo- and regioselective sialylation of inositol. A key phosphodiester linkage between the mono-, di-, and trisialyl inositols and ceramide was formed at a late state employing the phosphoramidite method.
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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com