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New ruthenium-based protocol for cleavage of terminal olefins to primary alcohols: Improved synthesis of a bicyclic nucleoside

Author
SHARMA, Pawan K1 ; NIELSEN, Poul1
[1] Nucleic Acid Center, Department of Chemistry, University of Southern Denmark, 5230 Odense, Denmark
Source

Journal of organic chemistry. 2004, Vol 69, Num 17, pp 5742-5745, 4 p

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)
Alcool primaire Clivage Composé bicyclique Composé éthylénique Diol Nucléoside Oléfine Oxydation Réduction chimique Sodium Periodate Sodium Tétrahydroborate Synthèse chimique Thymine dérivé Dihydroxylation Pyrimidine-2,4-dione(1-[1-hydroxy-2-hydroxyméthyl-3,6-dioxabicyclo[3.2.0]hept-4-yl]-5-méthyl) Ruthénium VIII Oxyde
Keyword (en)
Primary alcohol Cleavage Bicyclic compound Ethylenic compound Diol Nucleoside Olefin Oxidation Chemical reduction Sodium Periodates Sodium Tetrahydroborates Chemical synthesis Thymine derivatives
Keyword (es)
Alcohol primario Clivaje Compuesto bicíclico Compuesto etilénico Diol Nucleósido Olefina Oxidación Reducción química Sodio Periodato Sodio Borohidruro Síntesis química Timina derivado
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
16032778

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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