Enantiospecific synthesis of 3,4-disubstituted glutamic acids via controlled stepwise ring-opening of 2,3-aziridino-γ-lactone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
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2. (b) Moloney, M. G. Nat. Prod. Rep. 1999, 16, 485–498;
3. (c) Doble, A. Pharmacol. Ther. 1999, 81, 163–221.
4. For recent examples, see: (a) Bunch, L.; Johansen, T. H.; Bräuner-Osborne, H.; Stensbøl, T. B.; Johansen, T. N.; Krogsgaard-Larsen, P.; Madsen, U. Bioorg. Med. Chem. 2001, 9, 875–879;
5. (j) Wermuth, C. G.; Mann, A.; Schoenfelder, A.; Wright, R. A.; Johnson, B. G.; Burnett, J. P.; Mayne, N. G.; Schoepp, D. D. J. Med. Chem. 1996, 39, 814–816;
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