Synthesis of carbocyclic 2',3'-dideoxy-2'-C-hydroxymethyl nucleosides as potential inhibitors of HIV
- Author
- ROSENQUIST, Å1 ; KVARNSTRÖM, I1 ; SVENSSON, S. C. T1 ; CLASSON, B; SAMUELSSON, B
[1] Linköping univ., dep. chemistry, 581 83 Linköping, Sweden - Source
Journal of organic chemistry. 1994, Vol 59, Num 7, pp 1779-1782
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité biologique Antiviral Composé monocyclique Diol In vitro Purine nucléoside Virus immunodéficience humaine Adénine(9-[2,4-bis(hydroxyméthyl)cyclopentyl]) Cyclopentane-1,2-dicarboxylique acide(3-oxo) ester diméthyle Cyclopentane-1,3-diméthanol(4-t-butoxycarbonylamino) diacétate Guanine(9-[2,4-bis(hydroxyméthyl)cyclopentyl]) Orthoformique acide ester triméthyle Pyrimidine(amino-4,6-dichloro) Lentivirinae Retroviridae Virus
- Keyword (en)
- Biological activity Antiviral Monocyclic compound Diol In vitro Purine nucleoside Human immunodeficiency virus Lentivirinae Retroviridae Virus
- Keyword (es)
- Actividad biológica Antiviral Compuesto monocíclico Diol In vitro Purina nucleósido Human immunodeficiency virus Lentivirinae Retroviridae Virus
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C07 Carbohydrates. Nucleosides and nucleotides / 001C03C07B Nucleosides, nucleotides and oligonucleotides
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4004091
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1021/jo00086a031 
https://dx.doi.org/10.1021/jo00086a031
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