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Advantages of fluoroformates as carboalkoxylating reagents for polar reactants

Author
VU ANH DANG1 ; OLOFSON, R. A
[1] Pennsylvania state univ., dep. chemistry, University Park CA 16802, United States
Source

Journal of organic chemistry. 1990, Vol 55, Num 6, pp 1851-1854 ; ref : 19 ref

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 Alcoxylation Alditol Aldose Amine tertiaire Composé bicyclique Diholoside Groupe protecteur Halogénoester Hétérocycle azote Oside polymère Pyrimidine nucléoside Vinylique alcool polymère Cellulose Formique acide(fluoro) ester alkyle Glucose Indolecarbaldéhyde-3 Saccharose Thymidine
Keyword (en)
Alcohol Alkoxylation Alditol Aldose Tertiary amine Bicyclic compound Disaccharide Protecting group Haloester Nitrogen heterocycle Polysaccharide Pyrimidine nucleoside Polyvinylalcohol
Keyword (es)
Alcohol Alcoxilación Alditol Aldosis Amina terciaria Compuesto bicíclico Diholosido Grupo protector Haloester Heterociclo nitrógeno Osido polímero Pirimidina nucleósido Vinílico alcohol polímero
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03A General

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
6842643

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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