Reversed-phase thin-layer chromatography of stereodefined 2-alkylidene-4-oxothiazolidines and 1,2-dithioles

Journal of Planar Chromatography - Modern TLC

Volumn 17, Issue 5, 2004, Pages 323-327

  Natić, Maja ^a   Marković, Rade ^a   Andelković, Katarina ^a   Milojković Opsenica, Dušanka ^a   Tešić, Živoslav ^a  

^a UNIVERSITY OF BELGRADE   (Serbia)

Author keywords

1,2 diothioles; 2 alkylidene 4 oxothiazolidines; Lipophilicity; Reversed phase TLC

Indexed keywords

ACETONE; BINARY MIXTURES; DATA REDUCTION; FURAN RESINS; METHANOL; SILICA; STEREOCHEMISTRY; THIN LAYER CHROMATOGRAPHY; WATER;

LIPOPHILICITY; ORGANIC MODIFIERS; REVERSED-PHASE THIN-LAYER CHROMATOGRAPHY; TETRAHYDROFURAN;

ORGANIC COMPOUNDS;

1,2 DITHIOLE DERIVATIVE; 2 ALKYLIDENE 4 OXOTHIAZOLIDINE DERIVATIVE; ACETONE; METHANOL; SILICON DIOXIDE; TETRAHYDROFURAN; THIAZOLIDINE DERIVATIVE; THIOL DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CALCULATION; CHEMICAL MODIFICATION; CONTROLLED STUDY; CORRELATION FUNCTION; DATA ANALYSIS; DRUG STRUCTURE; EXPERIMENTATION; INSTRUMENT; LINEAR SYSTEM; LIPOPHILICITY; REVERSED PHASE LIQUID CHROMATOGRAPHY; STEREOCHEMISTRY; THIN LAYER CHROMATOGRAPHY;

EID: 9744220434     PISSN: 09334173     EISSN: None     Source Type: Journal    
DOI: 10.1556/JPC.17.2004.5.1     Document Type: Article

References (22)

1. V.M. Timoshenko, J.-P. Bouillon, Y.G. Shermolovich, and C. Portella, Tetrahedron Lett. 43 (2002) 5809-5812.
2. S. Rajappa, Tetrahedron 55 (1999) 7065-7114.
3. S.P. Singh, S.S. Parmar K. Raman, and V.I. Stenberg, Chem. Rev. 81 (1981) 175-203.
4. Y. Martin, Quantitative Drug Design, Medicinal Research Series No. 8, Marcel Dekker, New York, 1978.
5. P. Magee, Chemtech 11 (1981) 378-384.
6. R. Smyth, M. Pfeffer D. Van Harken, A. Cohen, and G. Hottendorf, Antimicrob. Agents Chemother. 10 (1981) 1004-1012.
7. D. Koblin, E. Eger II, B. Johnson, P. Collins, R. Terrell, and L. Spears, Anesth. Analg. 60 (1981) 464-470.
8. H. Levitan, Proc. Natl Acad. Sci. USA 74 (1977) 2914-2918.
9. W. Neeley, D. Branson, and G. Blau, Environ. Sci. Technol. 8 (1974) 1113-1115.
10. E. Coats, G. Genther S. Dietrich, Z. Guo, and C. Hansch J. Med. Chem. 24 (1981) 1422-1429.
11. C. Tanford, The Hydrophobic Effect, 2nd edn, Wiley, New York, 1980, Chapter 13.
12. T. Slawik and B. Paw, J. Planar Chromatogr. 16 (2003) 442-446.
13. R. Marković, M. Baranac, and S. Jovetić, Tetrahedron Lett. 59 (2003) 5833-5836.
14. E.C. Bate-Smith and R.G. Westall, Biochim. Biophys. Acta 4 (1950) 427-440.
15. C. Hansch and A. Leo, Substituent Constants for Correlation Analysis in Chemistry and Biology, Wiley, New York, 1979.
16. milog P1.2, Molinspiration Property Calculation Service FAQ, http://www.molinspiration.com/
17. CSlog P, ChemSilico, http://www.chemsilico.com/
18. C.A. Lipinski, F. Lombardo, B.W. Dominy, and P.J. Feeney, Adv. Drug Delivery Rev. 23 (1997) 4-25; http://www.log P.com/
19. E. Soczewiński and C.A. Wachtmeister, J. Chromatogr. 7 (1962) 311-320.
20. K. Dross, Ch. Sonntag, and R. Mannhold, J. Chromatogr. 673 (1994) 113-124.
21. M.L. Bieganowska, A. Doraczynska, and A. Petruczynska, J. Planar Chromatogr. 8 (1995) 1282-1289.
22. R. Marković, A. Shirazi, Z. Džambaski, and M. Baranac, D. Minić, J. Serb. Chem. Soc. 68(1) (2003) 1-8.