Carbohydrate Chemistry Volume 24 by R J Ferrier; R Blattner; R H Furneaux

By R J Ferrier; R Blattner; R H Furneaux

Carbohydrate Chemistry offers overview assurance of all courses proper to the chemistry of monosaccharides and oligosaccharides in a given yr. the quantity of analysis during this box showing within the natural chemical literature is expanding due to the better value of the topic, specially in components of medicinal chemistry and biology. In no a part of the sphere is that this extra obvious than within the synthesis of oligosaccharides required by means of scientists operating in glycobiology. Clycomedicinal chemistry and its reliance on carbohydrate synthesis is now rather well validated, for instance, learn more... summary: Carbohydrate Chemistry presents assessment insurance of all courses suitable to the chemistry of monosaccharides and oligosaccharides in a given yr. the volume of analysis during this box showing within the natural chemical literature is expanding end result of the improved significance of the topic, particularly in parts of medicinal chemistry and biology. In no a part of the sphere is that this extra obvious than within the synthesis of oligosaccharides required via scientists operating in glycobiology. Clycomedicinal chemistry and its reliance on carbohydrate synthesis is now rather well demonstrated, for instance

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Indica, Chem, 1988,14, 255. (Chem. , 1990,112, 119 250). Mahaderappa, Carbohyir. , 1990,197, 119. 71 72 73 J. Li and S. Feng, Chem. Ind. (London), 1989, 423 (Chem Abstr.. 1990,112,20 658). Sauter and C. Makowka. Res. , 1989,302,411 (Chem. , 1990,112, 7 093). P. A. K. Kudelin, J. , 1990,112,7 199). H. McGall, J. W. Kozarich, J. Am. Chem. ,1990,112,3203. J. L. N. Richards, Carbow. , 1990,199, 111. J. L. Richards, Carbohydr. , 1990,199, 91. A. , 1990, 201, 311. K. Van der Eycken, M. Vandewalle, and H.

Reducing disaccharides are now treated according to their non-reducing units. "7 A novel and highly stereoselective method of making 1,2ck-related glycosides involves the use of 1,2-trans-related glycosyl thiocyanates with non-participating groups at C-2. l19 The triphenylsilyl group can be used to protect the anomeric hydroxyl group during disaccharide synthesis and can be removed selectively in the presence of functions such as the p-nitrobenzoyl. lm 3: Glycosides 31 Several developments have taken place in the synthesis of 1,2-trans-related compounds.

Larionov, k Y a . A. Goryacheva, Zh. , 1989,63, 2960 (Chem. Abstr. 1990,112,217 372). E. G. Larionov, and AYa. Pronin, Zh. , 1989,63,2%5 (Chem. , 1990,112,217373). L. Mega, S. L Van Etten, J. Org. , 1990,55,522. S. Chiba and A. Kimura, Agric. Biol. 54, 3023. O. K. Chae, Bull. Korean Chem. , 1990,11,183 (Chem. , 1990,113,172 467). E. G. Larionov, and AYa. Pronin, Zh. Fiz. , 1989,63,2716(Chem. , 1990,112,139 661). J. Serianni, and T. Vuorinen, Carbohydr. , 1990,206,1. W. Lichtenthaler and S. Ronninger, J.

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