Synthèse énantiosélective d'hexadiène -1,5 ols-3 tertiaires substitués en position 5 et 6 : étude de leur transposition d'Oxy-Cope
- Other title
- Enantioselective synthesis of 5- and 6-substituted tertiary 1,5-hexadiene-3ols. Study of oxy-cope transposition (en)
- Author
- MAS, Jean-Manuel
Lyon 1 (Degree-grantor) - Source
Synthèse énantiosélective d'hexadiène -1,5 ols-3 tertiaires substitués en position 5 et 6 : étude de leur transposition d'Oxy-Cope. 1986, 155 f.-pl, ref : 54 ref
- Thesis number
- 86 LYO1 0013
- Scientific domain
- Chim. organ
- Document type
- Thesis (Engineer's Ph.D. thesis)
- Language
- French
- Keyword (fr)
- Alcool tertiaire Composé aliphatique Composé diénique Composé énynique Cycle 3 chaînons Décyclisation Enantiomère Enantiosélectivité Epoxyde Hétérocycle oxygène Racémique Réaction catalytique Réaction sigmatrope Régiospécificité Stéréosélectivité Transposition Cope Cyclohexène-«3»ol(butyl-«3» éthyl-«4» heptyl-«1») Epoxydation Octadiène-«1,5»ol-3(butyl-«5» heptyl-«3») Oxiranne(alkyl-2 vinyl-«2») Oxiranne(heptyl-«2» vinyl-«2») Tridécène-«1»one-6(butyl-«2» éthyl-«3»)
- Keyword (en)
- Tertiary alcohol Aliphatic compound Dienic compound Enynic compound Three membered ring Ring cleavage Enantiomer Enantioselectivity Epoxide Oxygen heterocycle Racemate Catalytic reaction Sigmatropic reaction Regiospecificity Stereoselectivity Cope rearrangement
- Keyword (es)
- Alcohol terciario Compuesto alifático Compuesto diénico Compuesto enínico Ciclo 3 eslabones Deciclización Enantiómero Enantioselectividad Epóxido Heterociclo oxígeno Racémico Reacción catalítica Reacción sigmatrópica Regiospecificidad Estereoselectividad Transposición Cope
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C02 Aliphatic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7497390
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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Europe PubMed Central access
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