Potassium tert-butoxide promoted annulation of 2-alkynylphenyl propargyl ethers: Selective synthesis of benzofuran and 12H-benzoannulene derivatives

Journal of Organic Chemistry

Volumn 78, Issue 21, 2013, Pages 11017-11031

  Grimaldi, Tamiris B ^a   Back, Davi F ^a   Zeni, Gilson ^a  

^a FEDERAL UNIVERSITY OF SANTA MARIA   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ANNULATION REACTIONS; FUNCTIONALIZED; OPTIMIZED REACTION CONDITIONS; POTASSIUM TERT-BUTOXIDE; PRODUCT FORMATION; PROPARGYL ETHERS; ROOM TEMPERATURE; SELECTIVE SYNTHESIS;

ETHERS; FUNCTIONAL GROUPS;

POTASSIUM;

12H BENZOANNULENBENZO[B]FURAN DERIVATIVE; 12H BENZOANNULENE DERIVATIVE; 2 ALKYNYLPHENYL PROPARGYL ETHER; 3 (3 METHYLBENZYL) 2 (PHENYLETHYNYL)BENZOFURAN; 3 (4 CHLOROBENZYL) 2 (PHENYLETHYNYL)BENZOFURAN; 3 (4 METHOXYBENZYL) 2 (PHENYLETHYNYL)BENZOFURAN; 3 (4 METHYLBENZYL) 2 (PHENYLETHYNYL)BENZOFURAN; 3 BENZYL 2 (4 TOLYLETHYNYL)BENZOFURAN; 3 BENZYL 2 (8 TOLYLETHYNYL)BENZOFURAN; 3 BENZYL 2 (NAPHTHALEN 1 YLETHYNYL)BENZOFURAN; 3 BENZYL 2 (NAPHTHALEN 2 YLETHYNYL)FURO[3,2 B]PYRIDINE; 3 BENZYL 2 (PHENYLETHYNYL)BENZOFURAN; 3 BENZYL 2 (PHENYLETHYNYL)FURO[3,2 B]PYRIDINE; 3 BENZYL 2 (THIOPHEN 3 YLETHYNYL)BENZOFURAN; 3 BENZYL 2 [(3 METHOXYPHENYL)ETHYNYL]BENZOFURAN; 3 BENZYL 2 [(4 CHLOROPHENYL)ETHYNYL) 5 METHYLBENZOFURAN; 3 BENZYL 2 [(4 CHLOROPHENYL)ETHYNYL]BENZOFURAN; 3 BENZYL 2 [(4 CHLOROPHENYL)ETHYNYL]FURO[3,2 B]PYRIDINE; 3 BENZYL 2 [(4 FLUOROPHENYL)ETHYNYL]BENZOFURAN; 3 BENZYL 2 [(4 METHOXYPHENYL)ETHYNYL]BENZOFURAN; 3 BENZYL 2 ALKYNYLBENZOFURAN DERIVATIVE; 3 BENZYL 2 ETHYNYLBENZOFURAN; 3 BENZYL 5 METHOXY 2 (PHENYLETHYNYL)BENZOFURAN; 3 BENZYL 5 METHYL 2 (PHENYLETHYNYL)BENZOFURAN; 3 PENTYL 2 (PHENYLETHYNYL)BENZOFURAN; ANNULENE DERIVATIVE; BENZOFURAN DERIVATIVE; POTASSIUM; POTASSIUM TERT BUTOXIDE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ALKYLATION; ANNULATION REACTION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTRON; ROOM TEMPERATURE; SONOGASHIRA REACTION;

EID: 84887121317     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo4020062     Document Type: Article

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