Synthesis and absolute stereochemistry of thysanone

Tetrahedron Letters

Volumn 40, Issue 20, 1999, Pages 3921-3924

  Donner, Christopher D ^a   Gill, Melvyn ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

Absolute stereochemistry; HRV 3C protease inhibitor; Hysanone; Synthesis

Indexed keywords

PROTEINASE INHIBITOR; QUINONE DERIVATIVE; THYSANONE; UNCLASSIFIED DRUG;

ARTICLE; DRUG CONFORMATION; DRUG SYNTHESIS; ENANTIOMER; PROTEINASE INHIBITION; STEREOCHEMISTRY; STRUCTURE ANALYSIS; X RAY CRYSTALLOGRAPHY;

EID: 0033553443     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00570-5     Document Type: Article

References (6)

1. 1. Part 53 in the series 'Pigments of Fungi'. For Part 52 see Aust. J. Chem., 1999, in press.
2. 2. S. B. Singh, M.G. Cordingley, R. G. Ball, J. L. Smith, A. W. Dombrowski and M. A. Goetz, Tetrahedron Lett., 1991, 32, 5279.
3. 3. J. M. Gwaltney Jr., in "Viral Infection of Man: Epidermicology and Control" 2nd Edtn, 1982, E. A. Evans (Ed.), Plenum Publishing Co., New York, pp. 491-517.
4. 4. C. Dimitriadis, M. Gill and M. F. Harte, Tetrahedron: Asymmetry, 1997, 8, 2153.
5. 13C NMR data for 1 were recorded on a JEOL JNM GX-400 spectrometer. Assignments in the spectra of the synthetic compound were confirmed by the results of HMQC and HMBC experiments.
6. 2