Issue 0, 1983

A general method for the preparation of 2-benzylpyrroles by modified borohydride reduction of azafulvenium salts

Abstract

2-Benzylpyrroles (5a–h) can be prepared in high yield from pyrroles by reduction, with modified borohydride reagents, of the corresponding 1-azafulvenium salts (3a–h) generated in situ in the presence of excess of phosphoryl trichloride. The procedure is compatible with ester groups.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1983, 633-636

A general method for the preparation of 2-benzylpyrroles by modified borohydride reduction of azafulvenium salts

G. McGillivray and E. Smal, J. Chem. Soc., Perkin Trans. 1, 1983, 633 DOI: 10.1039/P19830000633

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