Opening of 2',3'-O-anhydro-ring of 2',3'-O-anhydro-lyxo-uridine by alkyl- and arylamines. Easy syntheses and preparative uses of 2'-deoxy-2'-alkylamino-xylo- and 3'-deoxy-3'-alkylamino-ara-uridines-Reference-Cited by-同舟云学术

Opening of 2',3'-O-anhydro-ring of 2',3'-O-anhydro-lyxo-uridine by alkyl- and arylamines. Easy syntheses and preparative uses of 2'-deoxy-2'-alkylamino-xylo- and 3'-deoxy-3'-alkylamino-ara-uridines

Published:1995-01 Issue:5 Volume:51 Page:1459-1470
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bera Sanjib,Pathak Tanmaya,Langley Graham J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Inhibitory effect of 2',3'-didehydro-2',3'-dideoxynucleosides on infectivity, cytopathic effects, and replication of human immunodeficiency virus

2. HIV Inhibitors Targeted at the Reverse Transcriptase

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1. ChemInform Abstract: Opening of 2′,3′-O-Anhydro-ring of 2′,3′-O-Anhydro-lyxo-uridine by Alkyl- and Arylamines. Easy Syntheses and Preparative Uses of 2′-Deoxy- 2′-alkylamino-xylo- and 3′-Deoxy-3′-alkylamino-ara-uridines.;ChemInform;2010-08-17

2. A general and efficient route to 3′-deoxy-3′-N-, S-, and C-substituted altropyranosyl thymines from 2′,3′-O-anhydro-mannopyranosylthymine;Tetrahedron;2007-01

3. 3′-N-Alkylamino-3′-deoxy-ara-uridines: A new class of potential inhibitors of ribonuclease A and angiogenin;Bioorganic & Medicinal Chemistry;2006-02

4. Formation of 4’,5’-Didehydro-5’-deoxy-3’-O-methyluridine via Regioselective Nucleophilic Addition of Methoxide Anion to 2’,3’-Anhydro-5’-dehydro-5’-iodouridine;HETEROCYCLES;2006

5. A Diastereoselective and General Route to 5-Amino-5-deoxysugars: Influence of C-3 Substitution on the Addition of Amines to C-5 of Vinyl Sulfone-Modified Hex-5-enofuranosyl Carbohydrates;The Journal of Organic Chemistry;2005-09-01