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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1982 (1982), S. 265-274 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Di- and Polyamino Sugars, XXVIII1). - Substitution Reactions of 2-Amino-2-deoxy-α-D-gluco-pyranosides at Position 3Nucleophilic substitutions of N-protected 2-amino-2-deoxy-3-O-mesyl-α-D-glucopyranosides with azide ions were severely restricted by neighboring group participations. N-acetyl as blocking group (2) led to the formation of the oxazoline 3 while from N-dinitrophenyl derivatives (9; 17) isomeric products (10, 11; 18, 19) were formed via epimines. Structure proofs were given by spectroscopy as well as by independent syntheses.
    Notes: Nucleophile Substitutionen an N-geschützten 2-Amino-2-desoxy-3-O-mesyl-α-D-glucopyranosiden mit Azid-Ionen wurden durch Nachbargruppenreaktionen behindert. N-Acetyl als Schutz-gruppe (2) führte zum Oxazolin 3, aus Dinitrophenyl-Derivaten (9; 17) wurden über Epimine isomere Produkte (10, 11; 18, 19) erhalten. Die Konstitutionsbeweise wurden sowohl anhand der Spektren als auch durch unabhängige Synthesen geführt.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1985 (1985), S. 477-484 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Di- and Polyamino Sugars, XXXI. - Substitution Reactions of 2-Amino-2-deoxy-β-D-glucopyranosides at Position 3Neighboring-group participations obstruct nucleophilic substitutions of N-protected 2-amino-2-deoxy-3-O-mesyl-β-D-glucopyranosides with azide ions. From the N-dinitrophenyl derivative 8 besides the allopyranoside 10 the isomeric products 9 and 11 are formed, the latter via the aziridine 15. The N-acyl derivatives 3 and 13 yield the allopyranosides 5 and 19 as well as the oxazoline 4. Structure proofs were given by spectroscopy and by independent syntheses.
    Notes: Nachbargruppenreaktionen stören die nucleophile Substitution von N-geschützten 2-Amino-2-desoxy-3-O-mesyl-β-D-glucopyranosiden mit Azid-Ionen. Das Dinitrophenyl-Derivat 8 liefert neben dem Allopyranosid 10 die isomeren Produkte 9 und 11 über das Aziridin 15. Die N-Acylderivate 3 und 13 liefern die Allopyranoside 5 und 19 sowie das Oxazolin 4. Die Konstitutionsbeweise wurden sowohl anhand der Spektren als auch durch unabhängige Synthesen geführt.
    Type of Medium: Electronic Resource
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