Sonochemical cleavage of 2-(bromomethyl)aziridines by a zinc–copper couple
- 1 January 1994
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 10,p. 1221-1222
- https://doi.org/10.1039/c39940001221
Abstract
1-Alkyl- and 1-arylmethyl-2-(bromomethyl)aziridines are readily cleaved by the sonochemical zinc–copper couple in aqueous methanol at room temp. to afford allylamines.Keywords
This publication has 10 references indexed in Scilit:
- Free radical-mediated ring expansion and related annulationsChemical Reviews, 1993
- Substituent control over the regiochemistry of ring opening of 2-aziridinylmethyl radicalsTetrahedron Letters, 1993
- 1-Alkenylcycloalkoxy radical chemistry. A two-carbon ring expansion methodologyThe Journal of Organic Chemistry, 1993
- A new synthesis of .alpha.- and .beta.-damascones from the ionones.The Journal of Organic Chemistry, 1992
- Pyrrolidines and allylic amines from radical-induced cleavage of aziridinesTetrahedron, 1992
- Cleavage of 2,3-epoxyalkylhalides by the sonochemical zinc–copper coupleJournal of the Chemical Society, Chemical Communications, 1991
- Free radical cyclisation of unsaturated epoxidesTetrahedron, 1989
- Cyclisations of allyloxy radicalsTetrahedron Letters, 1988
- Radical-induced ring opening of epoxides. A convenient alternative to the wharton rearrangementJournal of the Chemical Society, Perkin Transactions 1, 1981
- AziridinemethanolsThe Journal of Organic Chemistry, 1970