Formal (3+2) Cycloaddition Reactions of 1-Methyl-2-(methylthio-(trimethylsilylmethylimino)methylimino)-1,2-dihydropyridine and Related Compound with Carbonyl Compounds Promoted by Fluoride Ion.
- 1 January 1995
- journal article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 43 (2) , 204-209
- https://doi.org/10.1248/cpb.43.204
Abstract
Reaction of 1-methyl-2-[methylthio(trimethylsilylmethylimino)methylimino]-1, 2-dihydropyridine (1), prepared from 2-amino-1-methyl-pyridinium iodide in 3 steps, with carbonyl compounds in the presence of 2 eq of cesium fluoride in acetonitrile afforded 2-(1-methyl-1, 2-dihydropyridylidene)aminooxazoline derivatives (12), which correspond to formal [3+2] cycloadducts of the aminonitrile ylid. Further, compound 1 reacted with carbonyl compounds in the presence of a catalytic amount of tetra-n-butylammonium fluoride (TBAF) to give corresponding cycloadducts.Keywords
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