An efficient friedel-crafts/oxa-michael/aromatic annulation: Rapid access to substituted naphtho[2,1-b]furan, naphtho[1,2-b]furan, and benzofuran derivatives

Chemistry - A European Journal

Volumn 19, Issue 13, 2013, Pages 4344-4351

  Anwar, Shaik ^a   Huang, Wan Yun ^a   Chen, Chih Hao ^a   Cheng, You Song ^a   Chen, Kwunmin ^a  

^a NATIONAL TAIWAN NORMAL UNIVERSITY   (Taiwan)

Author keywords

benzofurans; Friedel Crafts reaction; heterocycles; naphthofurans; nitroallylic acetate; synthetic methods

Indexed keywords

BENZOFURANS; HETEROCYCLES; NAPHTHOFURANS; NITROALLYLIC ACETATE; SYNTHETIC METHODS;

CYCLIZATION; FRIEDEL-CRAFTS REACTION; PHENOLS; RATE CONSTANTS; VOLATILE FATTY ACIDS;

ORGANIC POLLUTANTS;

BENZOFURAN DERIVATIVE; BIOLOGICAL PRODUCT; FURAN DERIVATIVE; NAPHTHALENE DERIVATIVE; NAPHTHO(2,1 B)FURAN; NAPHTHO(2,1-B)FURAN;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; SYNTHESIS;

BENZOFURANS; BIOLOGICAL AGENTS; CYCLIZATION; FURANS; MOLECULAR STRUCTURE; NAPHTHALENES; STEREOISOMERISM;

EID: 84875187709     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201204221     Document Type: Article

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