Iodobenzene-mediated intramolecular oxidative coupling of substituted 4-hydroxyphenyl-N-phenylbenzamides for the synthesis of spirooxindoles

Synthesis

Volumn , Issue 6, 2011, Pages 860-866

  Yu, Zhengsen ^a   Ju, Xuhui ^a   Wang, Junyan ^a   Yu, Wei ^a  

^a LANZHOU UNIVERSITY   (China)

Author keywords

hypervalent iodine; iodobenzene; oxidative coupling; phenolic coupling; spirooxindoles

Indexed keywords

HYPERVALENT IODINE; IODOBENZENE; OXIDATIVE COUPLING; PHENOLIC COUPLING; SPIROOXINDOLES;

INDUSTRIAL CHEMICALS; IODINE; PHENOLS;

SYNTHESIS (CHEMICAL);

1' BENZYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 3' CHLORO 1' METHYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 3' METHYL 1' METHYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 3' METHYLOXY 1' BENZYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 3' METHYLOXY 1' METHYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 4 HYDROXYPHENYL N PHENYLBENZAMIDE DERIVATIVE; 4' CHLORO 1' METHYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 5' CHLORO 1' METHYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' IND) 2',4 (1'H)DIONE; 5' CHLORO 1'BENZYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 5' ETHYLOXY 1' METHYL 4H SPIRO[CYCLOHEXA 2,5 DIENE 1,3' INDOL] 2',4 (1'H)DIONE; 5' FLUORO 1' BENZYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 5' METHYL 1' ALLYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 5' METHYL 1' BENZYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; 6' CHLORO 1' METHYL 4H SPIRO(CYCLOHEXA 2,5 DIENE 1,3' INDOL) 2',4 (1'H)DIONE; BENZAMIDE DERIVATIVE; INDOLE DERIVATIVE; IODOBENZENE; SPIROOXINDOLE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; AROMATIZATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; ELIMINATION REACTION; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 79952454866     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1259444     Document Type: Article

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