Synthesis of precursors for the dimeric 3-O-SO3Na Lewis X and Lewis A structures
✍ Scribed by Gurijala V. Reddy; Rakesh K. Jain; Robert D. Locke; Khushi L. Matta
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 895 KB
- Volume
- 280
- Category
- Article
- ISSN
- 0008-6215
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✦ Synopsis
Stereoselective syntheses of 3-O-SO3Na-beta-Gal-(1-->4)-beta-GlcNAc- (1-->3)-beta-Gal-(1-->4)-GlcNAc-beta-OBn (15) and 3-O-SO3Na-beta-Gal-(1-->3)-beta-GlcNAc-(1-->3)-beta-Gal-(1-->3)- beta-GlcNAc-(1-->3)-beta-Gal-(1-->4)-Glc-beta-OBn (25) were accomplished through the use of two novel glycosyl donors, namely, ethyl O-(2,6-di-O-acetyl-3,4-O-isopropylidene-beta-D- galactopyranosyl)-(1-->4)-3-O-acetyl-2-deoxy-2-phthalimido-1-thio-6-O- trimethylacetyl-beta-D-glucopyranoside (8). and ethyl O-(2,6-di-O-acetyl-3,4-O-isopropylidene-beta-D-galactopyranosyl)- (1-->3)-4-O-acetyl-2-deoxy-2-phthalimido-1-thio-6-O-trimethylace tyl-beta-D-glucopyranoside (18).
📜 SIMILAR VOLUMES
## Abstract The interaction of trimeric perfluoro‐__ortho__‐phenylene mercury (1) with carbazole in dichloromethane, THF, and THF/NEt~3~ leads to the crystallization of [1·C~12~H~8~NH] (2), [1·(C~12~H~8~NH·THF)] (3), and [1·(C~12~H~8~NH·NEt~3~)] (4), respectively. Adducts 3 and 4 have been characte