1,3-Dipolar cycloadditions of 2-thio-3-chloroacrylamides with nitrile oxides and nitrones
- Author
- KISSANE, Marie1 ; LAWRENCE, Simon E1 ; MAGUIRE, Anita R2
[1] Department of Chemistry, Analytical and Biological Chemistry Research Facility, University College Cork, Cork, Ireland
[2] Department of Chemistry & School of Pharmacy, Analytical and Biological Chemistry Research Facility, University College Cork, Cork, Ireland - Source
Tetrahedron (Oxford. Print). 2010, Vol 66, Num 25 ; 4409, 4564-4572 [10 p.] ; ref : 32 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Kidlington
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acrylamide Cycloaddition dipolaire 1,3 Décyclisation Dérivé de l'isoxazole Dérivé de la pipéridine Hétérocycle azote Hétérocycle oxygène azote Nitrile oxyde Nitrone Sulfure organique
- Keyword (en)
- Acrylamide 1,3-Dipolar cycloaddition Ring cleavage Isoxazole derivatives Piperidine derivatives Nitrogen heterocycle Oxygen nitrogen heterocycle Nitrile oxide Nitrone Organic sulfide
- Keyword (es)
- 1,3-Dipolar cicloadición Desciclización Piperidina derivado Heterociclo nitrógeno Heterociclo oxígeno nitrógeno Nitrilo óxido Nitrona Sulfuro orgánico
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- 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
- 22838534
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/j.tet.2010.04.057 
https://dx.doi.org/10.1016/j.tet.2010.04.057
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