Novel approach to 3,3-dimethyl-4-morpholino-3,4-dihydrocoumarins via hetero-Diels-Alder reaction

Tetrahedron

Volumn 70, Issue 35, 2014, Pages 5608-5618

  Mathur, Divya ^a,b   Prasad, Ashok K ^b   Cameron, T Stanley ^c   Jha, Amitabh ^a  

^a ACADIA UNIVERSITY   (Canada)

^b UNIVERSITY OF DELHI   (India)

^c DALHOUSIE UNIVERSITY   (Canada)

Author keywords

3,4 Dihydrocoumarins; Cascade reaction; Cyclization; Hetero Diels Alder; Inverse electron demand

Indexed keywords

2 (DIMORPHOLINOMETHYL) 4 FLUOROPHENOL; 2 (DIMORPHOLINOMETHYL) 4 METHYLPHENOL; 2 (DIMORPHOLINOMETHYL) 6 ETHOXYPHENOL; 2 (DIMORPHOLINOMETHYL) 6 METHOXYPHENOL; 2 (DIMORPHOLINOMETHYL) 6 METHYLPHENOL; 2 (DIMORPHOLINOMETHYL)PHENOL; 2 (DIPIPERIDIN 1 YLMETHYL)PHENOL; 2 [BIS(4 METHYLPIPERAZIN 1 YL)METHYL]PHENOL; 2,4 DICHLORO 6 (DIMORPHOLINOMETHYL)PHENOL; 3,3 DIMETHYL 2,4 DIMORPHOLINOCHROMAN; 3,3 DIMETHYL 4 MORPHOLINO 3,4 DIHYDROCOUMARIN DERIVATIVE; 3,3 DIMETHYL 4 MORPHOLINOCHROMAN 2 OL; 3,3,6 TRIMETHYL 2,4 DIMORPHOLINOCHROMAN; 3,3,6 TRIMETHYL 4 MORPHOLINOCHROMAN 2 OL; 3,3,8 TRIMETHYL 2,4 DIMORPHOLINOCHROMAN; 3,3,8 TRIMETHYL 4 MORPHOLINOCHROMAN 2 OL; 4 BROMO 2 (DIMORPHOLINOMETHYL)PHENOL; 4 CHLORO 2 (DIMORPHOLINOMETHYL)PHENOL; 6 BROMO 3,3 DIMETHYL 2,4 DIMORPHOLINOCHROMAN; 6 BROMO 3,3 DIMETHYL 4 MORPHOLINOCHROMAN 2 OL; 6 CHLORO 3,3 DIMETHYL 2,4 DIMORPHOLINOCHROMAN; 6 CHLORO 3,3 DIMETHYL 4 MORPHOLINOCHROMAN 2 OL; 6 FLUORO 3,3 DIMETHYL 2,4 DIMORPHOLINOCHROMAN; 6,8 DICHLORO 3,3 DIMETHYL 2,4 DIMORPHOLINOCHROMAN; 8 ETHOXY 3,3 DIMETHYL 2,4 DIMORPHOLINOCHROMAN; 8 ETHOXY 3,3 DIMETHYL 4 MORPHOLINOCHROMAN 2 OL; 8 METHOXY 3,3 DIMETHYL 2,4 DIMORPHOLINOCHROMAN; 8 METHOXY 3,3 DIMETHYL 4 MORPHOLINOCHROMAN 2 OL; COUMARIN DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ARTICLE; DEAMINATION; DIELS ALDER REACTION; ELECTRON; HYDROLYSIS; MICROWAVE IRRADIATION; NONHUMAN; ONE POT SYNTHESIS; OXIDATION; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REACTION ANALYSIS; REACTION TIME; STEREOCHEMISTRY; STOICHIOMETRY; TEMPERATURE;

ALNUS;

EID: 84949116781     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.06.083     Document Type: Article

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