Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/22374
Title: Synthesis of substituted cyclohex-2-enones
Authors: Ahmed, M G
Ahmed, SA
Romman, UK R
Akhter, K
Chowdhury, M A
Kiuchi, F
Issue Date: Aug-2001
Publisher: NISCAIR-CSIR, India
Abstract: Ethyl acetoacetate reacts with benzylideneacetone, 2-methoxy benzylideneacetone and furfurylideneacetone in the presence of sodium ethoxide as catalyst to yield 4-ethoxycarbonyl- 3-methyl-5-phenylcyclohex-2-enone 1a, 4-ethoxycarbonyl-3-methyl-5-(2-mcthoxyphenyl) cyclohex-2-enone 1b and 4-ethoxycarbonyl-5-(2-furanyl)-3-methylcyclohex-2-enone 1c, respectively. Ethyl benzoylacetate reacts with benzylideneacetone and furfurylideneacetone in the presence of sodium ethoxide to give 4-ethoxycarbonyl-3,5-bis-phenylcyclohex-2-enone 1d and 4-ethoxycarbonyl-5-(2-furanyl)-3-phenylcyclohex-2-enone 1e, respectively as products.
Page(s): 710-712
URI: http://hdl.handle.net/123456789/22374
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.40B(08) [August 2001]

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