Reactions of gem-Dihalophenylcyclopropanes with Nucleophilic Agents: Formation of Phenylcyclopropanone and 2-Phenylpropenal Acetals
Reactions of gem-dihalophenylcyclopropanes with alcohols in dimethyl sulfoxide in the presence of potassium tert-butoxide yield phenylcyclopropanone acetals. Reactions with alcohols in the presence of potassium hydroxide at 80-100°C yield cyclopropanone and 2-phenylpropenal acetals; their ratio depends mostly on the nature of the nucleophile.
Kostikov,Varakin,Molchanov,Ogloblin
p. 25 - 30
(2007/10/03)
A Novel Alkoxycyclopropene Ring-Opening Reaction
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Crossland, Ingolf
p. 310 - 312
(2007/10/02)
PRODUCTION OF 2-PHENYL-1-CYCLOPROPANONE ACETALS FROM 2,2-DIBROMO-1-PHENYLCYCLOPROPANE
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Varakin, G. S.,Kostikov, R. R.,Ogloblin, K. A.
p. 1569 - 1570
(2007/10/02)
Atropaldehyde
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Crossland, Ingolf
p. 6 - 6
(2017/05/06)
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