A simple and efficient method for the synthesis of amidophenols using iodine as catalyst under neat condition

Tetrahedron

Volumn 64, Issue 13, 2008, Pages 2972-2978

  Selvam, Nagarajan Panneer ^a   Perumal, Paramasivan T ^a  

^a CENTRAL LEATHER RESEARCH INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAMIDE DERIVATIVE; ACETONITRILE; LEWIS ACID; N [(2 HYDROXY NAPHTHALEN 1 YL) (2 HYDROXY PHENYL) METHYL] ACETAMIDE; N [(2,4 DICHLORO PHENYL) (2 HYDROXY PHENYL) METHYL] ACETAMIDE; N [(4 CHLORO PHENYL) (2 HYDROXY PHENYL) METHYL] ACETAMIDE; N [(4 NITRO PHENYL) (2 HYDROXY PHENYL) METHYL] ACETAMIDE; SODIUM THIOSULFATE; UNCLASSIFIED DRUG;

ACETYLATION; ARTICLE; CATALYST; HYDROGENATION; INFRARED SPECTROSCOPY; ONE POT SYNTHESIS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE; X RAY ANALYSIS;

EID: 39149136490     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.075     Document Type: Article

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23. Crystal structure of compound (entry 11, Table 1) has been deposited at the Cambridge Crystallographic Data Center and allocated the reference no. CCDC 651834.
24. Crystal structure of compound (entry 2, Table 1) has been deposited at the Cambridge Crystallographic Data Center and allocated the reference no. CCDC 651835.
25. Crystal structure of compound (entry 19, Table 1) has been deposited at the Cambridge Crystallographic Data Center and allocated the reference no. CCDC 652214.