Synthesis and characterization of 4-Aryl-4H-chromenes from H-cardanol

Natural Product Communications

Volumn 9, Issue 9, 2014, Pages 1333-1340

  Rao, Hulluru Surya Prakash ^a   Kamalraj, Mani ^a  

^a PONDICHERRY UNIVERSITY   (India)

Author keywords

4 Aryl 4H chromenes; Electrophilic substitution; H Cardanol; Nitroketene

Indexed keywords

1 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]NAPHTHALEN 2 OL; 2 (BENZYLOXY) 6 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]PHENOL; 2 METHYL 6 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]PHENOL; 2 [2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]NAPHTHALEN 1 OL; 2 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]PHENOL; 2 [6 BROMO 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [6 CHLORO 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [6 CHLORO 7 METHYL 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [6 ETHYL 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [6 METHOXY 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [6 METHYL 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL]5 PENTADECYLPHENOL; 2 [8 ETHOXY 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 2 [8 METHOXY 2 (METHYLAMINO) 3 NITRO 4H CHROMEN 4 YL] 5 PENTADECYLPHENOL; 4 ARYL 4H CHROMENE; 4 METHOXY 2 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]PHENOL; 5 CHLORO 2 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]PHENOL; 6 BROMO 1 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]NAPHTHALEN 2 OL; 7 METHOXY 1 [2 (METHYLAMINO) 3 NITRO 7 PENTADECYL 4H CHROMEN 4 YL]NAPHTHALEN 2 OL; CHROMENE DERIVATIVE; H CARDANOL; PHENOL; UNCLASSIFIED DRUG; BENZOPYRAN DERIVATIVE; CARDANOL; PHENOL DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CASHEW NUT; CATALYSIS; CHEMICAL ANALYSIS; ELECTROPHILICITY; HYDROGEN BOND; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; SUBSTITUTION REACTION; SYNTHESIS; ANACARDIUM; CHEMICAL STRUCTURE; CHEMISTRY;

ANACARDIUM; BENZOPYRANS; MOLECULAR STRUCTURE; PHENOLS;

EID: 84907522385     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1400900929     Document Type: Article

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