Synthesis of isonucleosides related to AZT and AZU
- Author
- PURDY, D. F; ZINTEK, L. B; VASU NAIR
Univ. Iowa, dep. chemistry, Iowa City IA 52242, United States - Source
Nucleosides & nucleotides. 1994, Vol 13, Num 1-3, pp 109-126 ; ref : 33 ref
- CODEN
- NUNUD5
- ISSN
- 0732-8311
- Scientific domain
- Biotechnology; Organic chemistry
- Publisher
- Dekker, Monticello, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité optique Alditol Argent Cyanate Composé chiral Cyclisation Didésoxynucléoside Lithium Azoture Milieu acide Pyrimidine nucléoside Régiosélectivité Acrylique acide(3-méthoxy-2-méthyl) chlorure Acrylique acide(3-éthoxy) chlorure Arabinitol(1,4-anhydro-3-azido-2,3-didésoxy-2-[1-thymyl]) Arabinitol(1,4-anhydro-3-azido-2,3-didésoxy-2-[uracil-1-yl]) Arabinitol(2-amino-1,4-anhydro-2-désoxy-3,5-O-[tétraisopropyldisiloxane-1,3-diyl]) Ribitol(1,4-anhydro)
- Keyword (en)
- Optical activity Alditol Silver Cyanates Chiral compound Cyclization Dideoxynucleoside Lithium Azides Acid medium Pyrimidine nucleoside Regioselectivity
- Keyword (es)
- Actividad óptica Alditol Plata Cianato Compuesto quiral Ciclización Didesoxinucleósido Litio Azoturo Medio ácido Pirimidina nucleósido Regioselectividad
- 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
- 4050536
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
10.1080/15257779408013230 
https://dx.doi.org/10.1080/15257779408013230
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