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Kinetic Resolution of Amines by a Nonenzymatic Acylation Catalyst We thank Michael M.-C. Lo, Dr. J. Craig Ruble, and Beata Tao for helpful discussions and preliminary studies, and we also thank Dr. George P. Luke (ARIAD Pharmaceuticals, Inc.) for providing the primary amine illustrated in entry 8 of Table 1. Support has been provided by Bristol-Myers Squibb, Merck, the National Institutes of Health (National Institute of General Medical Sciences, R01-GM57034), Novartis, Pfizer, and Pharmacia.
Arai S, Bellemin-Laponnaz S, Fu GC. Arai S, et al. Among authors: fu gc. Angew Chem Int Ed Engl. 2001 Jan 5;40(1):234-236. Angew Chem Int Ed Engl. 2001. PMID: 11169723 No abstract available.
Kinetic Resolution of Amines by a Nonenzymatic Acylation Catalyst We thank Michael M.-C. Lo, Dr. J. Craig Ruble, and Beata Tao for helpful discussions and preliminary studies, and we also thank Dr. George P. Luke (ARIAD Pharmaceuticals, Inc.) for providing the primary amine illustrated in entry 8 of Table 1. Support has been provided by Bristol-Myers Squibb, Merck, the National Institutes of Health (National Institute of General Medical Sciences, R01-GM57034), Novartis, Pfizer, and Pharmacia.
Arai S, Bellemin-Laponnaz S, Fu GC. Arai S, et al. Among authors: fu gc. Angew Chem Int Ed Engl. 2001 Feb 16;40(4):647. Angew Chem Int Ed Engl. 2001. PMID: 11241593 No abstract available.
Palladium-catalyzed coupling reactions of aryl chlorides.
Littke AF, Fu GC. Littke AF, et al. Among authors: fu gc. Angew Chem Int Ed Engl. 2002 Nov 15;41(22):4176-211. doi: 10.1002/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO;2-U. Angew Chem Int Ed Engl. 2002. PMID: 12434342 Review.
191 results