Enantioselective total synthesis of anti HIV-1 active (+)-calanolide A through a quinine-catalyzed asymmetric intramolecular oxo-Michael addition
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. Kashman, Y.; Gustafson, K. R.; Fuller, R. W.; Cardellina II, J. H.; McMahon, J. B.; Currens, M. J.; Buckheit Jr., R. W.; Hughes, S. H.; Cragg, G. M.; Boyd, M. R. J. Med. Chem. 1992, 35, 2735–2743; ibid. 1993, 36, 1110.
2. In vivo anti-HIV activity of (+)-calanolide a in the hollow fiber mouse model
3. Zembower, D. E.; Liao, S.; Flavin, M. T.; Xu, Z.-Q.; Stup, T. L.; Buckheit Jr., R. W.; Khilevich, A.; Mar, A. A.; Sheinkmann, A. K. J. Med. Chem. 1997, 40, 1005–1017 and references cited therein.
4. An approach to anti-HIV-1 active Calophyllum coumarin synthesis: An enantioselective construction of 2,3-dimethyl-4-chromanone ring by quinine-assisted intramolecular Michael-type addition
5. The details will be reported elsewhere.
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