Improvements in Diels-Alder cycloadditions with some acetylenic compounds under solvent-free microwave-assisted conditions: Experimental results and theoretical approaches

Tetrahedron

Volumn 60, Issue 7, 2004, Pages 1683-1691

  Loupy, André ^a   Maurel, François ^b   Sabatié Gogová, Andrea ^a,c  

^a CNRS   (France)

^b UNIVERSITÉ PARIS DIDEROT   (France)

^c SLOVAK UNIVERSITY OF TECHNOLOGY   (Slovakia)

Author keywords

Activation energy; Cycloaddition; Dipole moment; Microwave irradiation; Solvent free reaction

Indexed keywords

1,3 CYCLOHEXADIENE; 2 METHOXYTHIOPHENE; 2 PYRONE DERIVATIVE; 3 CARBOMETHOXY 2 PYRONE; ACETYLENE DERIVATIVE; ALKENE DERIVATIVE; SOLVENT; THIOPHENE DERIVATIVE; UNCLASSIFIED DRUG;

AB INITIO CALCULATION; ARTICLE; CYCLOADDITION; DIELS ALDER REACTION; HEATING; MICROWAVE RADIATION; PRIORITY JOURNAL; THEORETICAL STUDY;

BETULACEAE;

EID: 0742306818     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.11.042     Document Type: Article

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