Synthesis

Detritylation of N-tritylamines via a naphthalene-catalyzed lithiation process

C Behloul, D Guijarro, M Yus

Index: Behloul, Cherif; Guijarro, David; Yus, Miguel Synthesis, 2004 , # 8 p. 1274 - 1280

Full Text: HTML

Citation Number: 10

Abstract

Abstract The reaction of aliphatic and aromatic secondary and tertiary N-tritylamines 1 with lithium powder and a catalytic amount of naphthalene led to reductive detritylation, affording the corresponding amines 2 in good to excellent yields. The trityl group could selectively be removed in the presence of an allyl or a benzyl group. The detritylation process could successfully be extended to several hydroxy, alkoxy and amino functionalized N- ...

Related Articles:

Rhodium (III)-catalyzed N-nitroso-directed C–H olefination of arenes. High-yield, versatile coupling under mild conditions

[Kano, Shinzo; Tanaka, Yasuyuki; Sugino, Eiichi; Shibuya, Shiroshi; Hibino, Satoshi Synthesis, 1980 , # 9 p. 741 - 742]

More Articles...