Issue 0, 1972

1,1-Diphenylalkenes. Part II. Alkylation of 1,1-diphenylpropene carbanions. The principle of least motion

Abstract

Carbanions of the type [Ph2C[double bond, length as m-dash]CH[double bond, length as m-dash]CHR] were alkylated in liquid ammonia. A preponderance of α-alkylation occurred when R was H or Me, in accord with the principle of least motion. Contrary to predictions, exclusive α-alkylation occurred when R was Ph. The mechanism and synthetic utility of these reactions are discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1292-1295

1,1-Diphenylalkenes. Part II. Alkylation of 1,1-diphenylpropene carbanions. The principle of least motion

R. Boyce, W. S. Murphy and K. P. Klein, J. Chem. Soc., Perkin Trans. 1, 1972, 1292 DOI: 10.1039/P19720001292

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