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Issue 7, 1971
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Effect of substituents on the stereochemical course of Diels–Alder reaction between β-nitrostyrenes and trans,trans-1,4-diphenylbutadiene

Abstract

In a study of the Diels–Alder reaction of trans,-trans-1,4-diphenylbutadiene with β-nitrostyrenes a marked stereoselectivity to phenyl “endo” adducts has been observed on introduction of electron-withdrawing substituents in the para-position of the phenyl ring of the β-nitrostyrenes.

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Article type: Paper
DOI: 10.1039/C29710000303
Citation: J. Chem. Soc. D, 1971,0, 303-304

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    Effect of substituents on the stereochemical course of Diels–Alder reaction between β-nitrostyrenes and trans,trans-1,4-diphenylbutadiene

    P. C. Jain, Y. N. Mukerjee and N. Anand, J. Chem. Soc. D, 1971, 0, 303
    DOI: 10.1039/C29710000303

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