Synthetic Communications

A Simple Preparation of 2, 3, 4-Cyclopent-2-Enone

S Bernasconi, C Capellini, M Sisti

Index: Bernasconi,S. et al. Synthetic Communications, 1978 , vol. 8, p. 71 - 74

Full Text: HTML

Citation Number: 4

Abstract

Abstract During our approach to the total synthesis of pinguisone, 1 we required a convenient method for preparing 2, 3, 4-cyclopent-2-enone (I), to be tested as a dienophile in a Diels Alder reaction. Known methods2 are not fully satisfactory either for their poor yields or because the precursors are not easily available.

Related Articles:

Nazarov reaction of trisubstituted dienones: mechanism involving Wagner-Meerwein shift

[Motoyoshiya, Jiro; Yazaki, Toshikazu; Hayashi, Sadao Journal of Organic Chemistry, 1991 , vol. 56, # 18 p. 735 - 740]

Nazarov reaction of trisubstituted dienones: mechanism involving Wagner-Meerwein shift

[Motoyoshiya, Jiro; Yazaki, Toshikazu; Hayashi, Sadao Journal of Organic Chemistry, 1991 , vol. 56, # 18 p. 735 - 740]

Ferrocenic polyphosphines and polythioethers: synthesis, reactivity and structure

[Broussier, Roland; Ninoreille, Serge; Legrand, Corinne; Gautheron, Bernard Journal of Organometallic Chemistry, 1997 , vol. 532, # 1-2 p. 55 - 60]

Anodic oxidation. Part IX. Electrolysis of ethyl sodiomethylacetoacetate

[Brettle,R. et al. Journal of the Chemical Society [Section] C: Organic, 1970 , p. 1317 - 1320]

More Articles...