ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Inorganic Chemistry  (5)
  • Fucopyranosyl phosphate  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 3311-3324 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Functional Riburonic Acid DerivativesThe easily available methyl 2,3-O-isopropylidene-β-D-ribofuranosiduronic acid (2) is transformed into the corresponding dibenzyl- 5 and triacetyl compound 6 respectively. Both are appropriate starting materials for selective reactions at all positions of the riburonic acid frame. Selective cleavage of the benzyl groups of 5 delivers the ribofuranosyl halogenides 14-19 free of anomers via the 1-unprotected derivatives 10 and 11a-c. With N-nucleophiles derivatives are synthesized, which are useful for the formation of N-glycosides. The debenzylated compound 12 delivers the bridged lactone 13. Phosphorous pentachloride treatment of 6 leads to the 2-O-trichloroacetylribofuranosyl chloride derivative 21.
    Notes: Aus der bequem zugänglichen Methyl-2,3-O-isopropyliden-β-D-ribofuranosiduronsäure (2) wurden die entsprechenden Dibenzyl- und Triacetylderivate 5 bzw. 6 hergestellt, welche geeignete Ausgangsverbindungen für selektive Reaktionen an allen Positionen des Riburonsäuregerüsts sind. Durch selektive Abspaltung der Benzylgruppen aus 5 wurden über die 1-ungeschützten Derivate 10 und 11a-c die Ribofuranosylhalogenide 14-19 anomerenfrei isoliert. Mit N-Nucleophilen wurden daraus Derivate für die aufbauende Synthese von N-Glycosiden zugänglich. Aus der vollständig entbenzylierten Verbindung 12 wurde das überbrückte Lacton 13 erhalten. Phosphorpentachlorid-Behandlung von 6 lieferte das 2-O-Trichloracetylribofuranosylchlorid-Derivat 21.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1775-1789 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Stereospecific Synthesis of Nucleoside-5′-carboxylic Acid Derivatives with Pyrimidines as Hetero-cyclic BasePyrimidine nucleoside-5′-carboxylic acid derivatives were synthesized by condensation of riburonic acid glycosyl halides with heterocyclic bases via different methods. According to the investigations, the benzoyl-protected riburonic acid glycosyl halides 3b and 16b are valuable starting materials for the synthesis of β-nucleosides. Silver perchlorate proved to be the best catalyst in these condensation reactions with respect to stereoselectivity and yield. The methyl esters and the ethyl amides of uridine-, cytidine-, and thymidine-5′-carboxylic acid 8b, 11b, 18b, 19b and 20b were synthesized by this method stereospecifically and in good yield.
    Notes: Pyrimidinnucleosid-5′-carbonsäure-Derivate wurden durch Kondensation von Riburonsäure-glycosylhalogeniden mit heterocyclischen Basen nach verschiedenen Methoden hergestellt. Nach den Untersuchungen eignen sich als Ausgangskomponenten zur Synthese der β-Nucleoside am besten die benzoyl-geschützten Riburonsäure-glycosylhalogenide 3b und 16b. Die Verwendung von Silberperchlorat als Katalysator für die Kondensation ergab insgesamt die besten Ergebnisse bezüglich Stereoselektivität und Ausbeute. Die Methylester bzw. Ethylamide 8b, 11b, 18b, 19b und 20b der Uridin-, Cytidin- und Thymidin-5′-carbonsäure wurden auf diese Weise stereospezifisch und mit guten Ausbeuten synthetisiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 2834-2843 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Glycosylhydrazines, 5. Synthesis of pyrazole-, Pyrazolo[3,4-d]pyrimidine-, and 1H-1,2,4-Triazol-Nucleoside 5′-amide Derivatives via Riburonamide HydrazonesIn a single step reaction the 3,5-dimethylpyrazole nucleoside-5′-amides 6a,c, the functionally substituted pyrazole nucleoside-5′-amides 9a and 10b, and the 1H-1,2,4-triazol-nucleoside-5′-amide 18 were obtained regio- and stereoselectively from the riburonamide hydrazones 4a-c.9a and 10b were transformed into the unprotected pyrazolo[3,4-d]pyrimidine nucleoside-5-amide 14a and 15b, derivatives of allopurinol riboside. likewise the ethylamide 20 of virazole-5′-acid was synthesized from 18.
    Notes: Aus den Riburonamid-hydrazonen 4a-c wurden in einer Eintopfreaktion regio- und stereoselektiv die 5′-Säureamid-Derivate des 3,5-Dimethylpyrazol-nucleosids 6a,c, der funktionell substituierten Pyrazol-nucleoside 9a) und 10n) und des 1H-1,2,4-Triazole-nucleosids 18 direkt aufgebaut. Als Allopurinolribosid-Derivate wurden aus 9a und 10b die ungeschützten pyrazolo[3,4-d]pyrimidin-nucleosid-5′-säureamide 14a und 15b hergestellt. Entsprechend wurde aus 18 das Ethylamid 20, der Virazol-5′-säure erhalten.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0170-2041
    Keywords: Fucopyranosyl phosphate ; Fucose 1-phosphate ; Glycosyl phosphate ; GDP-fucose ; Guanosine diphosphofucose ; Trichloroacetimidates ; Carbohydrates ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of the benzyl- and acetyl-protected α-trichloroacetimidates 1 and 6α with dialkyl and diaryl phosphates in the presence of traces of acid affords stereoelectively the thermodynamically more stable α-L-fucopyranosyl phosphates 2, 7 and 8, respectively, in high yields. The use of very pure, recrystallized dibenzyl phosphate results in the stereoeletive formation of the β-L-fucopyranosyl phosphates 3 and 9. In each case separation of the anomers is not required because of the very high stereoselectivity of the reactions. After deprotection the fucose 1-phosphate 12 is coupled with GMP morpholidate 10 to yield GDP-fucose 13. After the development of a new purification procedure for GDP-fucose 13 we have obtained a very pure compound suitable for biochemical investigations. Analytical and preparative HPLC has been performed on reversed-phase columns using a volatile buffer system (triethylammonium hydrogen carbonate) as the eluant.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 70 (1937), S. 2415-2427 
    ISSN: 0365-9631
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 73 (1940), S. 980-983 
    ISSN: 0365-9631
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...