Issue 12, 1989

Stereoselective synthesis of (Rp)-benzylphenyl-[2-(S)-bromomethylpyrrolidine-1-yl]phosphine oxide from (S)-(+)-prolinol by the Michaelis–Arbuzov reaction: application in the synthesis of a chiral hybrid phosphine–phosphine oxide ligand

Abstract

The chiral oxazaphospholidine (2) derived from (S)-(+)-prolinol reacts with benzyl bromide in a stereoselective Michaelis–Arbuzov reaction to give (3), an ideal precursor for the synthesis of the chiral hybrid phosphine–phosphine oxide ligand (5).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 805-807

Stereoselective synthesis of (Rp)-benzylphenyl-[2-(S)-bromomethylpyrrolidine-1-yl]phosphine oxide from (S)-(+)-prolinol by the Michaelis–Arbuzov reaction: application in the synthesis of a chiral hybrid phosphine–phosphine oxide ligand

B. Faure, A. Archavlis and G. Buono, J. Chem. Soc., Chem. Commun., 1989, 805 DOI: 10.1039/C39890000805

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