An efficient synthesis of embelin derivatives through domino Knoevenagel hetero Diels-Alder reactions under microwave irradiation

Tetrahedron

Volumn 64, Issue 37, 2008, Pages 8938-8942

  Jiménez Alonso, Sandra ^a,b   Chávez, Haydee ^a,c   Estévez Braun, Ana ^a,b   Ravelo, Ángel G ^a,b   Feresin, Gabriela ^d   Tapia, Alejandro ^d  

^a UNIVERSIDAD DE LA LAGUNA   (Spain)

^b HOSPITAL UNIVERSITARIO NUESTRA SEÑORA DE CANDELARIA   (Spain)

^c Universidad Nacional San Luis Gonzaga   (Peru)

^d UNIVERSIDAD NACIONAL DE SAN JUAN   (Argentina)

Author keywords

Knoevenagel heteroDiels Alderreactions; Multicomponent reactions; MW irradiation; Quinones

Indexed keywords

2 ETHOXY 6 HYDROXY 7 UNDECYL 3,4 DIHYDRO 2H CHROMENE 5,8 DIONE; 6 HYDROXY 2 (2 PHENYLCYCLOHEXYLOXY) 7 UNDECYL 3,4 DIHYDRO 2H CHROMENE 5,8 DIONE; 6 HYDROXY 2 (2,4,6 TRIMETHYLPHENYL) 7 UNDECYL 3,4 DIHYDRO 2H CHROMENE 5,8 DIONE; 6 HYDROXY 2 PHENYL 7 UNDECYL 3,4 DIHYDRO 2H CHROMENE 5,8 DIONE; 6 HYDROXY 2 PHENYLSULFANYL 7 UNDECYL 3,4 DIHYDRO 2H CHROMENE 5,8 DIONE; 7 HYDROXY 8 UNDECYL 3,4,4A,10A TETRAHYDRO 2H 5H PYRANO[2,3 B]CHROMENE 6,9 DIONE; 8 HYDROXY 7 UNDECYL 4B,10,10A,11 TETRAHYDROINDENO[1,2 B]CHROMENE 6,9 DIONE; ALKENE; BENZOQUINONE DERIVATIVE; EMBELIN; NATURAL PRODUCT; PARAFORMALDEHYDE; PINENE; PYRAN DERIVATIVE; PYRANO 1,4 BENZOQUINONE DERIVATIVE;

ARTICLE; DIELS ALDER REACTION; ELECTRON; KNOEVENAGEL CONDENSATION; MICROWAVE IRRADIATION; MOLECULAR INTERACTION; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

ALNUS;

EID: 48049104329     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.06.057     Document Type: Article

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