On the synthesis of geminally functionalized heterocyclic aminocarboxylic acid esters
- Author
- COUTOULI-ARGYROPOULOU, E; THESSALONIKEOS, E
Univ. Thessaloniki, lab. organic chemistry, Thessaloniki 540 06, Greece - Source
Journal of heterocyclic chemistry. 1991, Vol 28, Num 8, pp 1945-1948 ; ref : 19 ref
- CODEN
- JHTCAD
- ISSN
- 0022-152X
- Scientific domain
- Organic chemistry
- Publisher
- HeteroCorporation, Odessa, FL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Carboxamide Cycle 5 chaînons Cycloaddition dipolaire 1,3 Hétérocycle azote Hétérocycle oxygène azote Méthanolyse Régiosélectivité Stéréosélectivité α-Aminoacide Isoxazole-5-carboxylique acide (3-aryl-5-benzamido-4,5-dihydro-4-phényl) ester méthyle Oxazol-5-one (3-benzylidène-4,5-dihydro-2-phényl) Pyrazole-5-carboxylique acide (3-aryl-5-benzamido-4,5-dihydro-4-phényl) ester méthyle
- Keyword (en)
- Carboxamide Five membered ring 1,3-Dipolar cycloaddition Nitrogen heterocycle Oxygen nitrogen heterocycle Methanolysis Regioselectivity Stereoselectivity α-Aminoacid
- Keyword (es)
- Carboxamida Ciclo 5 eslabones 1,3-Dipolar cicloadición Heterociclo nitrógeno Heterociclo oxígeno nitrógeno Metanólisis Regioselectividad Estereoselectividad α-Aminoácido
- 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
- 5056252
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
10.1002/jhet.5570280824 
https://dx.doi.org/10.1002/jhet.5570280824
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