Tetrahedron Letters p. 6565 - 6568 (1992)
Update date:2022-08-05
Topics:
Harms, Arthur E.
Stille, John R.
Treatment of alkyl titanocene chloride complexes with the Lewis acids EtAlCl2 or Me2AlCl resulted in intramolecular insertion of a tethered alkyne into the Ti-C bond.Regioselective alkyne insertion produced exocyclic trisubstituted alkene products resulting from four-, five-, and six-membered ring formation.In the case of cyclohexane formation, the alkyne was found to insert with syn stereoselectivity.
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