(Q63198376)

English

Synthesis of furo[2,3-c]pyran-β-d-nucleosides by radical-cyclization & their conformational analysis by 500 mhz 1h-nmr spectroscopy

No description defined

In more languages

edit

Statements

instance of

scholarly article

0 references

title

Synthesis of furo[2,3-c]pyran-β-d-nucleosides by radical-cyclization & their conformational analysis by 500 mhz 1h-nmr spectroscopy (English)

0 references

0 references

4

Jyoti Chattopadhyaya

0 references

author name string

Zhen Xi

series ordinal

1

0 references

Peter Agback

series ordinal

2

0 references

Anders Sandström

series ordinal

3

0 references

publication date

November 1991

0 references

published in

Tetrahedron

0 references

volume

47

0 references

issue

46

0 references

page(s)

9675-9690

0 references

cites work

Inhibition of infectivity of human immunodeficiency virus by a novel nucleoside, oxetanocin, and related compounds

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A ring-enlarged oxetanocin A analogue as an inhibitor of HIV infectivity

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis and evaluation of a series of 1-(3-alkyl-2,3-dideoxy-alpha,beta-D-erythro-pentofuranosyl)thymines

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Branched-chain sugar nucleosides. 3. 3'-C-methyladenosine

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Branched-chain sugar nucleosides. V. Synthesis and antiviral properties of several branched-chain sugar nucleosides

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Improved antitumor effects in 3'-branched homologs of 2'-deoxythioguanine. Synthesis and evaluation of thioguanine nucleosides of 2,3-dideoxy-3-(hydroxymethyl)-D-erythro-pentofuranose

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

New synthesis of 2',3'-dideoxy-3'-C-cyano-2'-substituted thymidines by michael addition reactions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Conformational studies op 3'--methyl and 2'--methyl analogues of cordycepin

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Radical deoxygenation of tert-alcohols in 2'-branched-chain sugar pyrimidine nucleosides: synthesis and antileukemic activity of 2'-deoxy-2' (S)-methylcytidine

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

New syntheses of 2',3'-dideoxy-2',3'-di-substituted & -2'-mono-substituted uridines & adenosines by michael addition reactions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Michael addition reactions of α β-ene-3′-phenylselenone of uridine. New synthesis of 2′,3′-dideoxy-ribo-aziridino-, 2′,3′-dideoxy-2′, 3′-ribo-cyclopropyl- & 2,2′-O-anhydro-3′-deoxy-3′-amino uridine derivatives

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis of new 2',3'-dideoxy-2',3'-α-fused-heterocyclic uridines, & some 2', 3'-ene-2'-substituted uridines from easily accessible 2',3'- ene-3'phenylselenonyl uridine

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis of new 2′, 3′-modified uridine derivatives from 2′,3′-ene-2′-phenylselenonyl uridine by Michael addition reactions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Intramolecular cyclization-trapping of carbon radicals by olefins as means to functionalize 2′- and 3′-carbons in β-D-nucleosides

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A new Synthesis of 1-(2,3-Dideoxy-β-D-Glycero-Pent-2-Enofuranosyl)- Thymine. A Highly Potent and Selective Anti-Hiv Agent

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Free-radical carbon-carbon bond formation in organic synthesis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Conformational analysis of the sugar ring in nucleosides and nucleotides. New description using the concept of pseudorotation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Conformational analysis of the sugar ring in nucleosides and nucleotides. Improved method for the interpretation of proton magnetic resonance coupling constants

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Inhibition of infectivity of human immunodeficiency virus by oxetanocin

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Derivatives of oxetanocin: oxetanocins H, X and G, and 2-aminooxetanocin A.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2991032-4

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0040-4020(01)91032-4

0 references

(Q63198376)

Synthesis of furo[2,3-c]pyran-β-d-nucleosides by radical-cyclization & their conformational analysis by 500 mhz 1h-nmr spectroscopy

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)