A New Route to Cyclic Amines by Anionic Cyclization

DOI: 10.1016/0040-4039(95)00200-V

Source and publish data:

Tetrahedron Letters p. 2157 - 2160 (1995)

Update date:2022-08-17

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Authors:

Coldham, Iain

Hufton, Richard

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Article abstract of DOI:10.1016/0040-4039(95)00200-V

Transmetallation of an aminomethylstannane gives rise to an aminomethyllithium which undergoes an anionic cyclization onto an unactivated alkene.The resulting organolithium reincorporates trimethyltin to give the product cyclic amine.The cyclization can b

Full text of DOI:10.1016/0040-4039(95)00200-V

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