Transition-metal catalysis in Michael addition of β-dicarbonyls: tuning of the reaction conditions
- Auteur
- KOCOVSKY, P1 ; DVORAK, D
[1] Czechoslovak acad. sci., inst. organic chemistry biochemistry, Prague 16610, Czechoslovakia - Source
Tetrahedron letters. 1986, Vol 27, Num 41, pp 5015-5018 ; ref : 16 ref
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Domaine scientifique
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Editeur
- Elsevier, Oxford
- Pays de publication
- United Kingdom
- Type de document
- Article
- Langue
- English
- Mot clé (fr)
- Addition Michaël Composé aliphatique Composé monocyclique Cycle 5 chaînons Cétoester Dicétone Enone Hétérocycle soufre Métal transition Complexe Réaction catalytique Acétylacétique acide,ester éthyle Borane(trifluoro) Cyclohexaneacétique acide(«α»-acétyl oxo-«3») ester éthyle Cyclohexène-«2»one Dioxanne Ethyle éther Ethylènedicarbaldéhyde-1,1([thiénylidène-3]-«2») Pentanedicarbaldéhyde-1,1(acétyl-«3» oxo-«4» [thiényl-«3»]-«2») Pentanedione-2,4
- Mot clé (en)
- Michael addition Aliphatic compound Monocyclic compound Five membered ring Ketoester Diketone Enone Sulfur heterocycle Transition metal Complexes Catalytic reaction
- Mot clé (es)
- Adición Michael Compuesto alifatico Compuesto monocíclico Ciclo 5 eslabones Cetoester Dicetona Enona Heterociclo azufre Metal transición Reacción catalítica
- Classification
- Pascal
- 001 Sciences exactes et technologie / 001C Chimie / 001C03 Chimie organique / 001C03C Préparations et propriétés / 001C03C05 Cyclanes, terpènes, prostaglandines, stéroïdes / 001C03C05A Cyclanes
- Discipline
- Organic chemistry
- Provenance
- Inist-CNRS
- Base de données
- PASCAL
- Identifiant INIST
- 8080311
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
10.1016/S0040-4039(00)85121-7 
https://dx.doi.org/10.1016/S0040-4039(00)85121-7
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