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Volumn 58, Issue 5, 2002, Pages 997-1003
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High chemoselectivity in microwave accelerated intramolecular domino Knoevenagel hetero Diels-Alder reactions - An efficient synthesis of pyrano[3-2c]coumarin frameworks
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Author keywords
Chromones; Coumarins; Diels Alder reactions; Microwave heating
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Indexed keywords
4 HYDROXY ALPHA NAPHTHOCOUMARIN;
4 HYDROXY BETA NAPHTHOCOUMARIN;
4 HYDROXYCOUMARIN;
[4A,12B] 2,5,5 TRIMETHYL 1,2,3,4,4A,12B HEXAHYDRO 1H [2]BENZOPYRANO[3 2C]COUMARIN;
ALDEHYDE DERIVATIVE;
ALKENE DERIVATIVE;
CITRONELLAL;
COUMARIN DERIVATIVE;
POLYCYCLIC HYDROCARBON;
PYRANOCOUMARIN DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL BINDING;
CHEMICAL REACTION;
CHEMICAL REACTION KINETICS;
DOMINO KNOEVENAGEL HETERO DIELS ALDER REACTION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
FRAMEWORK;
MICROWAVE IRRADIATION;
PRENYLATION;
PRIORITY JOURNAL;
X RAY CRYSTALLOGRAPHY;
BETULACEAE;
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EID: 0037185358
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)01076-6 Document Type: Article |
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Times cited : (71)
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References (18)
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