Enantioselective synthesis of the carbocyclic moiety of (−)-carbovir
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. A Concise Enantioselective Pathway to Carbocyclic Nucleoside: Asymmetric Synthesis of Carbocyclic Moiety of Carbovir
2. An asymmetric synthesis of (−)-carbovir
3. For synthesis of (−)-carbovir, see: (a) Vince, R.; Brownell, J. Biochem. Biophys. Res. Commun. 1990, 168, 912–916;
4. (b) Exall, A. M.; Jones, M. F.; Mo, C.-L.; Myers, P. L.; Paternoster, I. L.; Singh, H.; Storer, R.; Weingarten, G. G.; Williamson, C.; Brodie, A. C.; Cook, J.; Lake, D. E.; Meerholz, C. A.; Turnbull, P. J.; Highcock, R. M. J. Chem. Soc., Perkin Trans. 1 1991, 2467–2477;
5. (c) Jones, M. F.; Myers, P. L.; Robertson, C. A.; Storer R.; Williamson, C. J. Chem. Soc. Perkin Trans. 1 1991, 2479–2484;
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