Carbohydrate Chemistry: v. 10, Edition: 1st Edition. by J.S. Brimacombe

By J.S. Brimacombe

Carbohydrate Chemistry presents evaluation insurance of all guides appropriate to the chemistry of monosaccharides and oligosaccharides in a given yr. the volume of study during this box showing within the natural chemical literature is expanding as a result of the more advantageous significance of the topic, in particular 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 way of scientists operating in glycobiology. Clycomedicinal chemistry and its reliance on carbohydrate synthesis is now rather well confirmed, for instance, by means of the training of particular carbohydrate- dependent antigens, in particular cancer-specific oligosaccharides and glycoconjugates. insurance of themes comparable to nucleosides, amino-sugars, alditols and cyclitols additionally covers a lot examine of relevance to organic and medicinal chemistry. every one quantity of the sequence brings jointly references to all released paintings in given parts of the topic and serves as a complete database for the lively learn chemist. expert Periodical reviews offer systematic and exact evaluate assurance in significant parts of chemical examine. Compiled through groups of prime professionals within the appropriate topic parts, the sequence creates a different carrier for the lively examine chemist, with commonplace, in-depth money owed of growth specifically fields of chemistry. topic insurance inside assorted volumes of a given identify is the same and booklet is on an annual or biennial foundation.

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1976, 46, 97. S. Czernecki, C. Georgoulis, and C. Provelenghiou, Tetrahedron Letters, 1976, 3535. P. J. Garegg, T. Iversen, and S. , 1976, 50, C12. J. M. Kuster, H. Luftmann, and I. Dyong, Chem. , 1976, 109, 2223. E. , 1976, 48, 299. J. Kuster, I. Dyong, and D. Schmeer, Chem. , 1976, 109, 1253. g. lG3 The structures of 3-0-[(R)-l -carboxyethyl]-~-rhamnose,a constituent of the 0-antigenic lipopolysaccharide of Sh. dysenteriae type 165 4-O-[(S)-l-carboxyethyl]-~-glucose,a constituent of the extracellular polysaccharide material from Aerococcus viridans var.

KUSOV, V. A. Petrenko, and N. K. Kochetkov, Izuest. Akad. , Ser. , 1976, 887 (Chem. , 1976,85, 108 900n). V. N. Shibaev, Yu. Yu. Kusov, and V. A. Petrenko, Izuest. Akad. , Ser. , 1975, 1843 (Chem. , 1976, 84, 31 3192). L. L. Danilov, L. V. Volkova, and R. P. Evstigneeva, Zhur. ,1975, 45, 2307 (Chem. , 1976, 84, 105 919n). L. L. Danilov, L. V. Volkova, V. A. Bondarenko, and R. P. Evstigneeva, Bioorg. , 1975, 1, 905 (Chem. , 1976, 84, 105 921p). M. A. Grum-Grzhimailo, L. V. Volkova, and R. P. Evstigneeva, Zhur.

Demuth, Z . , 1976, 31b, 267. Glycosides 23 flavonoid C-glycosides (from Swertia perennis L. ) 140-143 have been characterized. A Wittig reaction has been used in an improved large-scale synthesis of the C-glycofuranoside derivative (32),144and the C-glycoside analogue (33) has been Reagents : i, Ph%MeLi+; ii, o::* Scheme 9 synthesized by the reactions shown in Scheme 9145 (see also the section on C-nucleosides in Chapter 21). Glycofuranosyl cyanides are dealt with in Chapter 7. lQ4 K. Hostettmann and A.

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