DBU-mediated regioselective intramolecular cyclization/dehydration of ortho diketo phenoxyethers: A synthesis of 2,3-substituted γ-benzopyranones

Tetrahedron

Volumn 69, Issue 44, 2013, Pages 9335-9348

  Bensulong, Sofia ^b   Boonsombat, Jutatip ^a   Ruchirawat, Somsak ^a,b  

^a CHULABHORN RESEARCH INSTITUTE   (Thailand)

^b THAILAND CENTER OF EXCELLENCE IN PHYSICS   (Thailand)

Author keywords

Benzofuran; Benzopyran; Benzopyranone; Isoflavone; Regioselective cyclization

Indexed keywords

BENZOFURAN DERIVATIVE; BENZOPYRAN DERIVATIVE; BICYCLO COMPOUND; DIETHYL 3 BENZOYLBENZOFURAN 2,6 DICARBOXYLATE; DIETHYL 4 OXO 3 PHENYL 4H CHROMENE 2,7 DICARBOXYLATE; DIETHYL BENZOFURAN 2,6 DICARBOXYLATE; ETHER DERIVATIVE; ETHYL 2 (2 (2 (3,4 DIMETHOXYPHENYL) 2 OXOACETYL)PHENOXY)ACETATE; ETHYL 2 (2 (2 (4 METHOXYPHENYL) 2 OXOACETYL)PHENOXY) ACETATE; ETHYL 2 (2 (2 OXO 3 (TETRAHYDRO 2H PYRAN 2 YLOXY)PROPANOYL)PHENOXY)ACETATE; ETHYL 2 (2 (2 OXOHEXANOYL)PHENOXY)ACETATE; ETHYL 3 (2 ETHOXY 2 OXOETHOXY) 4 (2 OXO 2 PHENYLACETYL)BENZOATE; ETHYL 3 (2 METHOXYPHENYL) 4 OXO 4H CHROMENE 2 CARBOXYLATE; ETHYL 3 (3,4 DIMETHOXYBENZOYL) 4,6 DIMETHOXYBENZOFURAN 2 CARBOXYLATE; ETHYL 3 (3,4 DIMETHOXYBENZOYL)BENZOFURAN 2 CARBOXYLATE; ETHYL 3 (3,4 DIMETHOXYPHENYL) 4 OXO 4H CHROMENE 2 CARBOXYLATE; ETHYL 3 (3,4 DIMETHOXYPHENYL) 4 OXO 7 (TOSYLOXY) 4H CHROMENE 2 CARBOXYLATE; ETHYL 3 (4 METHOXYBENZOYL)BENZOFURAN 2 CARBOXYLATE; ETHYL 3 (4 METHOXYPHENYL) 4 OXO 4H CHROMENE 2 CARBOXYLATE; ETHYL 3 BENZOYLBENZOFURAN 2 CARBOXYLATE; ETHYL 3 BUTYL 4 OXO 4H CHROMENE 2 CARBOXYLATE; ETHYL 3 BUTYL 6 METHOXY 4 OXO 4H CHROMENE 2 CARBOXYLATE; ETHYL 3 PIVALOYLBENZOFURAN 2 CARBOXYLATE; ETHYL 4 OXO 3 ((TETRAHYDRO 2H PYRAN 2 YLOXY)METHYL) 4H CHROMENE 2 CARBOXYLATE; ETHYL 4 OXO 3 PHENYL 4H CHROMENE 2 CARBOXYLATE; ETHYL 4 OXO 3 PHENYL 7 (TOSYLOXY) 4H CHROMENE 2 CARBOXYLATE; ETHYL 6 NITRO BENZOFURAN 2 CARBOXYLATE; ETHYL 7 METHOXY 3 (4 METHOXYPHENYL) 4 OXO 4H CHROMENE 2 CARBOXYLATE; ETHYL 7 METHOXY 4 OXO 3 PHENYL 4H CHROMENE 2 CARBOXYLATE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL PARAMETERS; CONTROLLED STUDY; CYCLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; SUBSTITUTION REACTION;

EID: 84884417627     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.07.104     Document Type: Article

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