Optically active cyclopropanols by samarium(II) iodide induced intramolecular reductive cyclisation of β-chloro-substituted amides
- Author
- FADEL, A
CNRS Univ. Paris-Sud, inst. chimie moléculaire Orsay, lab. carbocycles, 91405 Orsay, France - Source
Tetrahedron : asymmetry (Print). 1994, Vol 5, Num 4 ; VII, 531-534 [5 p.]
- ISSN
- 0957-4166
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier Science, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité optique Alcool tertiaire Composé chiral Composé monocyclique Cycle 5 chaînons Cyclopropanation Hétérocycle oxygène azote Réaction catalytique Réaction intramoléculaire Samarium II Iodure Cyclopropanol dérivé Oxazolidin-2-one(4-benzyl-3-[2-chlorométhyl-3,3-diméthylbutyryl]) Chlore Composé organique
- Keyword (en)
- Optical activity Tertiary alcohol Chiral compound Monocyclic compound Five membered ring Cyclopropanation Oxygen nitrogen heterocycle Catalytic reaction Intramolecular reaction Samarium II Iodides Chlorine Organic compounds
- Keyword (es)
- Actividad óptica Alcohol terciario Compuesto quiral Compuesto monocíclico Ciclo 5 eslabones Ciclopropanación Heterociclo oxígeno nitrógeno Reacción catalítica Reacción intramolecular Samario II Ioduro Cloro Compuesto orgánico
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4008195
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
10.1016/0957-4166(94)80010-3 
https://dx.doi.org/10.1016/0957-4166(94)80010-3
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