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Straightforward synthesis of enantiomerically pure (3S, 4R)- and (3R, 4S)-3,4-isopropylidenedioxypyrroline 1-oxide, precursors of functionalized cis-dihydroxy azaheterocycles, by a novel one-pot procedure

Author
CICCHI, Stefano1 ; CORSI, Massimo1 ; BRANDI, Alberto1 ; GOTI, Andrea1
[1] Dipartimento di Chimica Organica Ugo Schiff, Centro di Studio C.N.R. sulla Chimica e la Struttura dei Composti Eterociclici e loro Applicazioni (CSCEA), Università degli Studi di Firenze, via della Lastruccia 13, 50019 Sesto Fiorentino, Firenze, Italy
Source

Journal of organic chemistry. 2002, Vol 67, Num 5, pp 1678-1681 ; ref : 14 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)
Composé chiral Hydroxylamine organique Hétérocycle oxygène azote Nitrone Réaction one pot Synthèse asymétrique Synthèse chimique 1,3-Dioxolo[4,5-c]pyrrole(2,2-diméthyl-4,6a-dihydro)-5-oxyde Dioxolopyrrole Furo[3,4-d][1,3]dioxol-4-ol(2,2-diméthyl-tétrahydro) Furodioxole
Keyword (en)
Chiral compound Organic hydroxylamine Oxygen nitrogen heterocycle Nitrone One pot reaction Asymmetric synthesis Chemical synthesis
Keyword (es)
Compuesto quiral HIdroxilamina orgánica Heterociclo oxígeno nitrógeno Nitrona Reacción one pot Síntesis asimétrica Síntesis química
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
13534524

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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