Synthesis, regioselective hydrogenolysis, partial hydrogenation, and conformational study of dioxane and dioxolane-type (9'-anthracenyl)methylene acetals of sugars.
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Anikó Borbás | András Lipták | I. Komáromi | A. Borbás | A. Mándi | S. Antus | László Lázár | István Komáromi | L. Lázár | Zsolt Jakab | Attila Mándi | Attila Bényei | Sándor Antus | A. Lipták | A. Bényei | Z. Jakab
[1] G. Sheldrick. A short history of SHELX. , 2008, Acta crystallographica. Section A, Foundations of crystallography.
[2] S. Oscarson. Protective Group Strategies , 2007 .
[3] A. Borbás,et al. 1.06 – Protecting Group Manipulations in Carbohydrate Synthesis , 2007 .
[4] D. Levy,et al. The organic chemistry of sugars , 2005 .
[5] U. Ellervik. 9-Anthraldehyde acetals as protecting groups. , 2003 .
[6] S. Pérez,et al. Experimental proof for the structure of a thrombin-inhibiting heparin molecule. , 2001, Chemistry.
[7] E. Toone,et al. Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3·Et2O , 2000 .
[8] Louis J. Farrugia,et al. WinGX suite for small-molecule single-crystal crystallography , 1999 .
[9] A. Borbás,et al. Synthesis and Hydrogenolysis of Dioxolane-Type Diphenyl-Methylene and Fluoren-9-Ylidene Carbohydrate Acetals Containing a Neighbouring Substituted Hydroxyl Function , 1997 .
[10] F. A. Luzzio,et al. 2,2′-Bipyridinium chlorochromate/m-chloroperbenzoic acid-mediated cleavage of cyclic acetals to hydroxyesters☆ , 1997 .
[11] K Schulten,et al. VMD: visual molecular dynamics. , 1996, Journal of molecular graphics.
[12] Giovanni Luca Cascarano,et al. Completion and refinement of crystal structures with SIR92 , 1993 .
[13] A. Borbás,et al. Hydrogenolysis of Dioxolane-Type Diphenylmethylene Acetals by AlClH2 to Axial Diphenylmethyl Ethers , 1993 .
[14] Tetsutaro Igarashi,et al. Oxidative Cleavage of 4,6-O-Benzylidene Ring with t-Butyl Hydroperoxide and Copper(II) Chloride. Preparation of Methyl 4-O- and 6-O-Benzoylhexopyranoside Derivatives , 1988 .
[15] R. Gigg,et al. The reaction of O-protected glycosides of 2-benzamido-2-deoxy-β-D-glucose with trimethylsilyl chloride–sodium hydride and subsequent reduction with lithium aluminium hydride☆ , 1982 .
[16] R. Gigg,et al. The Allyl Group for Protection in Carbohydrate Chemistry. 13. The N-Allylbenzylamino Group for Protection in the Amino-Sugar Series , 1982 .
[17] H. Hultberg,et al. A novel, reductive ring-opening of carbohydrate benzylidene acetals, with unusual regioselectivity , 1981 .
[18] P. Kováč,et al. Hydrogenolysis of 3,5-0-benzylidene acetals with the LiAlH4-AlCl3 reagent in methyl d-xylofuranosides , 1981 .
[19] P. Nánási,et al. 13C-N.m.r. relaxation times and chemical shifts of the exo and endo isomers of dioxolane-type benzylidene acetals of carbohydrates: determination of the absolute configuration , 1977 .
[20] D. Horton,et al. Reaction of derivatives of methyl 2,3-O-benzylidene-6-deoxy-α-L-mannopyranoside with butyllithium: Synthesis of methyl 2, 6-dideoxy-4-O-methyl-α-L-erytho-hexopyranosid-3-ulose , 1976 .
[21] P. Nánási,et al. Stereoselective ring-cleavage of 3-O-benzyl- and 2,3-di-O-benzyl-4,6-O-benzylidenehexopyranoside derivatives with the LiAlH4AlCl3, reagent , 1975 .
[22] A. B. Foster,et al. 617. Aspects of stereochemistry. Part XXII. Structure, conformation, and absolute configuration of some carbohydrate benzylidene acetals containing fused ring systems , 1965 .
[23] R. Lamb,et al. 286. The condensation of α-methylgalactoside with benzaldehyde , 1934 .
[24] J. Irvine,et al. LXV.—Partially methylated glucoses. Part II. βγ-Dimethyl α-glucose and βγ-dimethyl β-glucose , 1913 .