The synthesis of β-lactams via a one-pot Reformatsky reaction of imines promoted by Zn/Cp2TiCl2 (cat.)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. The Reformatsky Reaction with Benzalaniline
2. For β-lactam syntheses: (a) van der Steen, F. H.; van Koten, G. Tetrahedron 1991, 47, 7503; (b) Ghosez, L.; Marchand-Brynaert, S. Formation of Four-membered Heterocycles. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, UK, 1991; Vol. 5, p. 85; (c) Hart, D. J.; Ha, D. C. Chem. Rev. 1989, 89, 1447; (d) Kawabata, T. Heteroat. Chem. 2000, 22, 33–58; (e) Palomo, C.; Cossio, F. P.; Arrieta, A.; Odriozola, J. M.; Oiarbide, M.; Ontoria, J. M. J. Org. Chem. 1989, 54, 5736.
3. Recent Advancements in the Reformatsky Reaction
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