7-(β-D-Arabinofuranosyl)-2, 4-dichlor-7H-pyrrolo[2,3-d]pyrimidin – Synthese, selektiver Halogenaustausch und Einfluß glyconischer Schutzgruppen auf die Reaktivität des Aglycons-Reference-Cited by-同舟云学术

7-(β-D-Arabinofuranosyl)-2, 4-dichlor-7H-pyrrolo[2,3-d]pyrimidin – Synthese, selektiver Halogenaustausch und Einfluß glyconischer Schutzgruppen auf die Reaktivität des Aglycons

Published:1984-04-12 Issue:4 Volume:1984 Page:722-733
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Seela Frank,Driler Hansjürgen

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference24 articles.

1. 2-Amino-7-(.beta.-D-arabinofuranosyl)pyrrolo[2,3-d]pyrimidin-4(3H)-one. Synthesis of ara-7-deazaguanosine via phase-transfer glycosylation

2. Selective 7-Glycosylation of 4-Amino-7H-pyrrolo[2,3-d]pyrimidine to Ara-Tubercidin and Its ?-Anomer

3. ara-7-Desazanebularin – Synthese eines fluoreszierenden Pyrrolo[2,3-d]pyrimidin-Nucleosids durch Phasentransferglycosylierung

4. und , Publikation in Vorbeeitung.

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