Publication Type:

Journal Article

Source:

Synthesis, Number 15, p.2466-2470 (2011)

URL:

http://www.scopus.com/inward/record.url?eid=2-s2.0-79960835419&partnerID=40&md5=9f4ba18d5a11566ea90baf3f6722449e

Keywords:

(2 ethoxy 4 hydroxy 5 phenylfuran 3 yl)phenylmethanone, (4 hydroxy 2, (4 hydroxy 2 methoxy 5 phenylfuran 3 yl)pyridin 3 ylmethanone, (4 hydroxy 2 methyl 5 phenylfuran 3 yl)phenylmethanone, 1, 1 ( 4 hydroxy 2 methyl 5 phenylfuran 3 yl)ethanone, 1(2 ethoxy 4 hydroxy 5 phenylfuran 3 yl)ethanone, 2 (4 chlorophenyl) 6, 2 (4 methoxyphenyl) 6, 2 biphenyl 4 yl 6, 3 dicarbonyl derivative, 3-dicarbonyl compounds, 5 diphenylfuran 3 yl)phenylmethanone, 6, 6 dimethyl 2 naphthalen 1 yl 6, 6 dimethyl 2 naphthalen 2 yl 6, 6 dimethyl 2 para tolyl 6, 6 dimethyl 2 phenyl 6, 6 dimethyl 6, 7 dihydrobenzofuran 4(5h) one, Acetylene, acetylene derivative, Ammonium compounds, Ammonium nitrate, Aromatic compounds, article, carbonyl derivative, Cerium, cerium ammonium nitrate, Cerium compounds, chemical reaction, chemical structure, ethyl 2 ethoxy 4 hydroxy 5 phenylfuran 3 carboxylate, furan derivative, Furan derivatives, isopropyl 4 hydroxy 2 isopropoxy 5 phenylfuran 3 carboxylate, Lighting, multisubstituted furans, Organic pollutants, oxidation, Oxidative additions, structure analysis, Terminal acetylene, terminal acetylenes, unclassified drug

Abstract:

Cerium(IV) ammonium nitrate mediated oxidative addition of 1,3-dicarbonyl compounds to terminal acetylenes to yield multisubstituted furan derivatives is reported here. The simplicity of the reaction and the ease of execution are particularly noteworthy. © Georg Thieme Verlag Stuttgart, New York.

Notes:

cited By (since 1996)3

Cite this Research Publication

Aa Sivan, Deepthi, Aa, and Nandialath, Vb, “Oxidative addition of 1,3-dicarbonyl compounds to terminal acetylenes mediated by cerium(IV) ammonium nitrate”, Synthesis, pp. 2466-2470, 2011.