Collection of Czechoslovak Chemical Communications - digital archive 

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• Jakubec Martin, Císařová Ivana, Karban Jindřich, Sýkora Jan: The Effect of Deoxyfluorination on Intermolecular Interactions in the Crystal Structures of 1,6-Anhydro-2,3-epimino-hexopyranoses. Molecules 2022, 27, 278. <https://doi.org/10.3390/molecules27010278>
• Karban Jindřich, Sýkora Jan, Kroutil Jiří, Císařová Ivana, Padělková Zdeňka, Buděšínský Miloš: Synthesis of All Configurational Isomers of 1,6-Anhydro-2,3,4-trideoxy-2,3-epimino-4-fluoro-β-d-hexopyranoses. J. Org. Chem. 2010, 75, 3443. <https://doi.org/10.1021/jo1000912>
• Sýkora Jan, Karban Jindřich, Císařová Ivana, Hilgard Stanislav: Molecular structure of eight possible configurational isomers of 2,3- and 3,4-epimino derivatives of 1,6-anhydro-β-d-hexopyranoses: conformation analysis, intra- and inter-molecular hydrogen bonds. Carbohydrate Research 2008, 343, 2789. <https://doi.org/10.1016/j.carres.2008.05.025>
• Karban Jindřich, Buděšínský Miloš, Kroutil Jiří: Synthesis of 1,6-Anhydro-2,3,4-trideoxy-2,3-epimino- and 1,6-Anhydro-2,3,4-trideoxy-3,4-epimino-β-D-hexopyranoses and Their NMR and Infrared Spectra. Collect. Czech. Chem. Commun. 2004, 69, 1939. <https://doi.org/10.1135/cccc20041939>
• Kroutil Jiřı́, Karban Jindřich, Buděšı́nský Miloš: Utilization of nosylepimines of 1,6-anhydro-β-d-hexopyranoses for the preparation of halogenated aminosaccharides. Carbohydrate Research 2003, 338, 2825. <https://doi.org/10.1016/j.carres.2003.07.003>
• Karban Jindřich, Buděšínský Miloš, Černý Miloslav, Trnka Tomáš: Synthesis and NMR Spectra of 1,6-Anhydro-2,3-dideoxy-2,3-epimino- and 1,6-Anhydro-3,4-dideoxy-3,4-epimino-β-D-hexopyranoses. Collect. Czech. Chem. Commun. 2001, 66, 799. <https://doi.org/10.1135/cccc20010799>
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• Černý Ivan, Buděšínský Miloš, Trnka Tomáš, Černý Miloslav: Preparation of 2-amino-1,6-anhydro-2,3-dideoxy-β-d-arabino-hexopyranose. 1H- and 13C-n.m.r. spectra of deoxy derivatives of 2-amino-1,6-anhydro-2-deoxy-d-glucose and 2-amino-1,6-anhydro-2-deoxy-d-mannose. Carbohydrate Research 1984, 130, 103. <https://doi.org/10.1016/0008-6215(84)85273-8>
• Reckendorf Wolfgang Meyer Zu, Lenzen Heinz‐Jürgen: Di‐ und Polyaminozucker, XXVIII1) Zur Substitution von 2‐Amino‐2‐desoxy‐α‐D‐glucopyranosiden in der 3‐Stellung. Liebigs Ann. Chem. 1982, 1982, 265. <https://doi.org/10.1002/jlac.198219820210>
• C̄erný Miloslav, C̄erný Ivan, Trnka Tomás̄: Ammonolysis of 1,6-anhydro-2,4-di-O-tosyl- β-d-glucopyranose and 1,6:3,4-dianhydro-2-O-tosyl-β-d-galactopyranose: preparation of 4-amino-1,6-anhydro-4-deoxy-β-d-manno- and -β-d-altro-pyranose. Carbohydrate Research 1978, 67, 33. <https://doi.org/10.1016/S0008-6215(00)83728-3>
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• Paulsen H., Koebernick H., Stenzel W., Köll P.: Darstellung von 2-azido-2-desoxy-d-glucopyranose und z, 4-diazido-2,4-didesoxy-d-glucopyranose. Tetrahedron Letters 1975, 16, 1493. <https://doi.org/10.1016/S0040-4039(00)72177-0>
• CERNY M., ELBERT T., PACAK J.: ChemInform Abstract: SYNTHESES WITH ANHYDRO SUGARS PART 21, PREPARATION OF 1,6‐ANHYDRO‐2,3‐DIDEOXY‐2,3‐EPIMINO‐BETA‐D‐MANNOPYRANOSE AND ITS CONVERSION TO 2‐AMINO‐1,6‐ANHYDRO‐2‐DEOXY‐BETA,D‐MANNOPYRANOSE. Chemischer Informationsdienst 1974, 5. <https://doi.org/10.1002/chin.197440445>