By R J Ferrier, R Blattner, O McDonald, R H Furneaux, P C Tyler, R H Wightman, K Clinch, J M Gardiner, R A Field, K P R Kartha, D M G Tilbrook
This product isn't really on hand individually, it's only bought as a part of a suite. There are 750 items within the set and those are all offered as one entity. summary: This product isn't really on hand individually, it's only offered as a part of a collection. There are 750 items within the set and those are all offered as one entity
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Extra info for Carbohydrate Chemistry Volume 32
Perez, Afinidad, 1998, 55, 51 (Chem. , 1998,128,321 812). P. Hadwiger, A. Lechner and A. Stiitz, J. Carbohydr. , 1198,17,241. P. Hadwiger and A. Stutz, J, Carbohydr. , 1198,17, 1259. 14 Carbohydrate Chemistry 41 Z. Hricoviniova, M. Hricovini, M. Petrusova, M. Matulova and L. Petrus, Chem. Pap,, 1998,52,238 (Chem. , 1998,129, 330 942). K. A. Begum and B. Pal, Carbohydr. , 1998,309,303. S. Singh, A. K. Singh and B. Singh, Transition Met. Chem. (London), 1998,23,277 (Chem. , 1998,129, 149 146). K.
J. Freudigmann, Tetrahedron, 1997, 53, 3669. 53 Y. Shigemasa, N. Tereda, T. Mori, M. Morimoto, H. Sashiwa and H. Saimoto, Bull. Chem. SOC. , 1998,71, 1 1 3. 1 Synthesis of Monosaccharides Glycosides. - A review has been published on papers dealing with solid-phase syntheses in organic chemistry (Part 111) which appeared during the period Nov 199GDec 1997. 1). I . I Methods of synthesis of glycosides. Some simple glycosides can be made directly from free sugars by novel approaches. ~ of D-glucose, D-galactose, D-mannose, D-glucuronic acid and D-galacturonic acid have been made with long chain alcohols in THF with Lewis acids such as BF3, FeC13, CaC12 as catalysts.
G. 2 Chain-extension at the 'Reducing End'. 30 OH I HO 49 Alkyl ketosides 53 were available by opening of the mixed spiroepoxides 52 with alcohols in the presence of ZnC12 (only a-anomers were produced). The isomeric mixture 52 was obtained by oxidation of the known em-glycal 51 with dimethyldioxirane, and a considerable improvement in the synthesis of 51 from lactone 50 by use of a Peterson olefination instead of reaction with Tebbe reagent has been r e p ~ r t e d . g. compounds 58, have been synthesized by ring-closing metathesis in the presence of Grubbs' catalyst, as illustrated in Scheme 5.