Carbohydrate Chemistry Volume 8 by C. S. And Wolfrom, M. L. (editors) Hudson

By C. S. And Wolfrom, M. L. (editors) Hudson

This product isn't really to be had individually, it is just 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 on hand individually, it's only bought as a part of a collection. There are 750 items within the set and those are all bought as one entity

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1974, 37, 75. K. L. , 1973, 31, 410. K. L. Matta, E. A. Z. Johnson, and J. J. , 1974, 32, 418. K. L. Matta, E. A. Z. Johnson, and J. J. , 1974, 32, 396. -R. Pougny and P. , 1974, 38, 161. S. Koto, K. Yago, S. Zen, and S . Omura, Bull. Chem. SOC. Japan, 1973, 46, 3800. N. K. Kochetkov, B. A. Dmitriev, 0. S. Chizhov, E. M. Klimov, N. N. Malysheva, V. I. Torgov, Ya. A. Chernyak, and N. E. Bairamova, Izuest. Akad. , Ser. , 1974, 1386. K. Takiura, M. Yamamoto, Y. Miyaji, H. Takai, S. Honda, and H.

Klemer, and H. , 1974, 36, 398. Okuda, K. Konishi, and S. Saito, Chem. and Pharm. Bull. (Japan), 1974, 22, 1624. J. C. Martin, J. A. Franz, and R. J. Arhart, J. Amer. Chem. ,1974, 96, 4604. 5 mol of sodium methoxide and this sulphonylating reagent also furnished the intermediate 2-toluene-p-sulphonate in high yield. Buchanan and his colleagues have extended their work on sugar epoxides in a report on the synthesis and properties of 2,3-anhydro-~-mannose and 3,4anhydro-D-altrose, which were obtained by hydrogenolysis of the corresponding benzyl g l y ~ o s i d e s .

B. Repke, and J. G . Moffatt, J . Org. , 1974, 39, 2176. J. M. J. Tronchet, A. -B. Zumwald, and F. Perret, Helu. Chim. Acta, 1974, 57 1505. K. Hostettman and A. Jacot-Guillarmod, Helu. Chim. A d a , 1974, 57, 204. M X . -L. Bouillant, G . Planche, and J. Chopin, Compr. , 1974, 279, C, 409. l~~ Isopropylidene and cyclohexylidene groups were shown to be stable under the conditions of demethylation, but benzylidene and benzyl ether groups were cleaved. It will be interesting to see whether the general utility of this reaction can be substantiated and whether a mechanistic rationale can be developed.

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