SYNTHESIS OF CYCLIC IMINES BY ADDITION OF GRIGNARD-REAGENTS TO OMEGA-BROMONITRILES

Authors
FRY DF FOWLER CB DIETER RK
Citation
Df. Fry et al., SYNTHESIS OF CYCLIC IMINES BY ADDITION OF GRIGNARD-REAGENTS TO OMEGA-BROMONITRILES, Synlett, (10), 1994, pp. 836-838
Citations number
30
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
10
Year of publication
1994
Pages
836 - 838
Database
ISI
SICI code
0936-5214(1994):10<836:SOCIBA>2.0.ZU;2-0
Abstract
Omega-Bromonitriles readily undergo a tandem addition-cyclization reac tion sequence with Grignard reagents at room temperature in hydrocarbo n/ether solvent mixtures to give good yields of 2-substituted pyrrolin es and tetrahydropyridines.