Issue 3, 1997
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Cycloaddition vs. conjugative Michael-type addition of 2-ethoxy-3-morpholinobuta-1,3-diene with nitroolefins

Gašper Marc,   Patrizia Nitti,   Giuliana Pitacco,   Alessandro Pizzioli  and  Ennio Valentin  

Abstract

The reactivity of the title dienamine towards conjugated nitroolefins has been investigated. With 1-nitrocyclopentene carbocyclic products largely predominated, whereas with 1-nitrocyclohexene only Michael-type products were formed. The behaviour of β-nitrostyrene was found to be dependent on the reaction conditions used.

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Article information

DOI
https://doi.org/10.1039/A605345I
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 223-228

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Cycloaddition vs. conjugative Michael-type addition of 2-ethoxy-3-morpholinobuta-1,3-diene with nitroolefins

G. Marc, P. Nitti, G. Pitacco, A. Pizzioli and E. Valentin, J. Chem. Soc., Perkin Trans. 1, 1997, 223 DOI: 10.1039/A605345I

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