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- The megalomicins. Part 7. A structural revision by carbon-13 nuclear magnetic resonance and X-ray crystallography. Synthesis and conformational analysis of 3-dimethylamino- and 3-azido-D- and -L-hexopyranosides, and the crystal structure of 4″-O-(4-lodobenzoyl)megalomicin A. Peter Bartner, Dena L. Boxler, Raymond Brambilla, Alan K. Mallams, James B. Morton, Paul Reichert, Frederick D. Sancilio, Henry Surprenant, Gregory Tomalesky, Gabor Lukacs, Alain Olesker, Ton That Thang, Lydia Valente, Satoshi Omura
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 1600
- Branched-chain sugars. Part 18. Syntheses of D-rubranitrose (2,3,6-trideoxy-3-C-methyl-4-O-methyl-3-nitro-D-xylo-hexopyranose) and a derivative of D-kijanose (2,3,4,6-tetradeoxy-4-methoxycarbonylamino-3-methyl-3-nitro-α-D-xylo-hexopyranose). John S. Brimacombe, Khandker M. M. Rahman
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 1073
- Synthesis of thiodisaccharides related to 4-thiolactose. Specific structural modifications increase the inhibitory activity against E. coli β-galactosidase. Lucas Dada, Juan Pablo Colomer, Verónica E. Manzano, Oscar Varela
, Org. Biomol. Chem.
, 2023
, 21
, 2188
- Kijanimicin. Part 3. Structure and absolute stereochemistry of kijanimicin. Alan K. Mallams, Mohindar S. Puar, Randall R. Rossman, Andrew T. McPhail, Ronald D. Macfarlane, Richard L. Stephens
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 1497
- Internal asymmetric induction by the C-6 substituent on the oxidation reaction of interglycosidic sulfur atom of thiodisaccharides. J. P. Colomer, A. B. Peñéñory, O. Varela
, RSC Adv.
, 2017
, 7
, 44410
- Chemical modification of trehalose. Part VI. The synthesis of analogues containing 2,2′-dideoxy-functions. L. Hough, A. C. Richardson, E. Tarelli
, J. Chem. Soc. C
, 1971
, 1732
- 856. Aspects of stereochemistry. Part XVI. Intramolecular hydrogen bonding in ethyl 2,3-dideoxy-α-D-erythro- and -threo-hexopyranosides and related compounds. A. B. Foster, R. Harrison, J. Lehmann, J. M. Webber
, J. Chem. Soc.
, 1963
, 4471
- Synthesis of derivatives of methyl 2,6-dideoxy-4-O-methyl-α-D-ribo-hexopyranoside: on the structure of variose. John S. Brimacombe, Annalee S. Mengech, Leslie C. N. Tucker
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 643
- Chemical modification of trehalose. Part VIII. The synthesis of 3,3′-dideoxy-analogues. L. Hough, A. C. Richardson, E. Tarelli
, J. Chem. Soc. C
, 1971
, 2122
- Syntheses of methyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside (methyl α-L-amicetoside) and methyl 2,3,4,6-tetradeoxy-4-(dimethylamino)-α-L-threo-hexopyranoside (methyl α-L-ossaminide). J. S. Brimacombe, L. W. Doner, A. J. Rollins
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2977