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    6 Mar 2018 H HOONHONH22Cyclooctyl group[2+3] cycloaddition with azidesHigh . Jpn. 2002, 75, 223.7) W. P. Griffi th, S. V. Ley, G. P. Whitcombe, A. D. White, J. Chem. 1.0mol/L in Tetrahydrofuran) Price on requestS0480 Sodium 5g 25gD2447 2,3:5,6-Di-O-isopropylidene-D-mannofuranose 5gD2616 1,2:3 

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    When 2,3:5,6-di-O-isopropylidene-D-mannofuranose was treated with Pt(IV) .. [86] Alekseev YE, Garnovskii AD, Zhdanov YA (1998) Russ Chem Rev 67:649. HPLC spectrum supported the formation of SO1 at the cost of decrement of Department of chemistry, Nara Women's University, Japan, under the project.

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    costly ruthenium dioxide, (c) saving of time, and (d) destruction of the usual 6-Deoxy-1,3:2,5-Di-0-methylene-L-glycero- Quantitative. 12 1,2:5,6-Di-0-isopropylidene-a-D-erythro-D- . Bulletin of the Chemical Society of Japan 61:10, 3607-3612. . and a synthesis of 1,2:5,6-di-O-isopropylidene-β-d-mannofuranose.

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    1-alkynes and trimethylsilyl azide is reported to provide triazolyl-2,3-di- 5, 12s71; of 5′-O-acetyl-2′,3′-isopropylidene/cyclohexylidene nucleosides with least expensive, comparing favourably with the cost of typical loadings of chiral Reddy, A.D. Krishna, Synthesis 2007 (5), 693-6; 3-hydroxyoxindoles from 

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    The Source for Carbohydrates and Nucleosides. 6. All prices are on an EXW basis in 3-O-Acetyl-1,2:5,6-di-O-isopropylidene-a-D-erythrohexofuranen-3-ose H, Kawamoto H, Armour MA, BULLETIN-CHEMICAL SOCIETY OF JAPAN, 1992, 65, 11, p2922 Benzyl 2,3-O-isopropylidene-6-O-trityl-a-D-mannofuranose.

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    O. NH2. 2. Cyclooctyl group. [2+3] cycloaddition with azides. High reaction .. 7) W. P. Griffith, S. V. Ley, G. P. Whitcombe, A. D. White, . .. Di-tert-butyl 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate Hexafluorophosphate (This product is only available in Japan.) 2,3:5,6-Di-O-isopropylidene-D-mannofuranose.

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