Highly selective cross-metathesis with phenyl vinyl sulphone using the ‘second generation’ Grubbs’ catalyst
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. For recent reviews, see the following for leading references: (a) Trnka, T. M.; Grubbs, R. H. Acc. Chem. Res. 2001, 34, 18–29; (b) Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012–3043; (c) Schrock, R. S. Tetrahedron 1999, 55, 8141–8153; (d) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413–4450; (e) Schuster, M.; Blechert, S. Angew. Chem., Int. Ed. Engl. 1997, 36, 2036–2055; (f) Fürstner, A. Top. Catal. 1997, 4, 285–299; (g) Ivin, K. J.; Mol, J. C. Olefin Metathesis and Metathesis Polymerization, 2nd ed.; Academic Press: New York, 1997.
2. Acrylonitrile Cross-Metathesis: Coaxing Olefin Metathesis Reactivity from a Reluctant Substrate
3. For a comprehensive survey of N-heterocyclic carbenes, see: (a) Bourissou, D.; Guerret, O.; Gabbaı̈, F. P.; Bertrand, G. Chem. Rev. 2000, 100, 39–91; (b) Arduengo, A. J. A. Acc. Chem. Res. 1999, 32, 913–921; (c) Herrmann, W. A.; Köcher, C. Angew. Chem., Int. Ed. Engl. 1997, 36, 2163–2187.
4. N-heterocyclic carbenes: novel ruthenium–alkylidene complexes
5. Highly Active Ruthenium Catalysts for Olefin Metathesis: The Synergy of N‐Heterocyclic Carbenes and Coordinatively Labile Ligands
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