Issue 12, 1971

Stereochemistry of a Michaelis–Arbusov reaction: alkylation of optically active ethyl trimethylsilyl phenylphosphonite with retention of configuration

Abstract

Ethylation of ethyl phenylphosphinate (I)via ethyl trimethylsilyl phenylphosphonite or via the corresponding trimethylstannyl ester, and free-radical addition of (I) to ethylene proceed with complete, or almost complete, retention of configuration.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 606-607

Stereochemistry of a Michaelis–Arbusov reaction: alkylation of optically active ethyl trimethylsilyl phenylphosphonite with retention of configuration

G. R. van den Berg, D. H. J. M. Platenburg and H. P. Benschop, J. Chem. Soc. D, 1971, 606 DOI: 10.1039/C29710000606

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