Synthesis 2005(17): 2946-2950  
DOI: 10.1055/s-2005-872168
PAPER
© Georg Thieme Verlag Stuttgart · New York

Zwitterionic Compounds in the Synthesis of Water-Soluble 1,3-Oxathiolane Derivatives

Barbara Zaleska*a, Marcin Karelusa, Ewelina Zadoraa, Hanna Kruszewskab
a Department of Organic Chemistry, Jagiellonian University, ul. Ingardena 3, 30-060 Kraków, Poland
Fax: +48(12)6340515; e-Mail: zaleska@chemia.uj.edu.pl;
b National Institute of Public Health, Department of Antibiotics and Microbiology, ul. Chemska 30/34, 00-725 Warszawa, Poland
Further Information

Publication History

Received 14 April 2005
Publication Date:
12 August 2005 (online)

Abstract

Perhydropyrimidin-2-ylium and perhydro-1,3-diazepin-2-ylium iodides with linked 1,3-oxathiolane ring were obtained. These new, water-soluble derivatives of 1,3-oxathiolane were prepared by cyclocondensation of diiodomethane with appropriate zwitterionic derivatives of 2-hydroxypropionic acid. The iodides were exploited in metathesis process with various anions.

    References

  • 1 Kramer W, Weissmueller J, Reiser W, Berg D, Brandes W, and Reinecke P. inventors; Ger Offen., DE  3420828.  ; Chem. Abstr. 1986, 104, 64212
  • 2 Angeli P. Gianella M. Pigini M. Gualtieri F. Teodori E. Valsecchi B. Givaraghi G. Eur. J. Med. Chem.  1985,  20:  517 
  • 3 Yokoyama M, Togo H, Kubo M, Baba K, Yamamoto Y, and Kudou M. inventors; Jpn. Kokai Tokkyo Koho, JP  1129567 (9929567).  ; Chem. Abstr. 1999, 130, 193113
  • 4 Belleau B, Belleau P, and Nguyen-Ba N. inventors; U.S. Patent, US  200120026.  ; Chem. Abstr. 2001, 135, 211232
  • 5 Mansour TS, and Jin H. inventors; U.S. Patent, US  6228860.  ; Chem. Abstr. 2001, 134, 336206
  • 6 Carroll SS, MacCoss M, Kuo LC, Olsen DB, Bhat B, Eldrup AB, Prhavc M, Malik L, and Bera S. inventors; PCT Int. Appl., WO  0320222.  ; Chem. Abstr. 2003, 138, 221789
  • 7 Gumina G. Song G.-Y. Chu CK. FEMS Microbiol. Lett.  2001,  202:  9 
  • 8 Mansour TS. Evans CA. Charron M. Korba BE. Bioorg. Med. Chem. Lett.  1997,  7:  303 
  • 9 Hirano H, Nakamura Y, Nagata H, and Tamura H. inventors; Jpn. Kokai Tokkyo Koho, JP  2001316386.  ; Chem. Abstr. 2001, 135, 357913
  • 10 Hirano H, Nakamura Y, Nagata H, and Tamura H. inventors; Jpn. Kokai Tokkyo Koho, JP  200139972.  ; Chem. Abstr. 2001, 134, 146752
  • 11 Djerassi C. Gorman M. J. Am. Chem. Soc.  1953,  75:  3704 
  • 12 Ralls JW. Dodson RM. Riegel B. J. Am. Chem. Soc.  1949,  71:  3320 
  • 13 Wilson GE. Huang MG. Schloman WW. J. Org. Chem.  1968,  33:  2133 
  • 14 Kamal A. Chouhan G. Ahmed K. Tetrahedron Lett.  2002,  43:  6947 
  • 15 Karimi B. Seradj H. Synlett  2000,  805 
  • 16 Blagoev M. Linden A. Heimgartner H. Helv. Chim. Acta  2000,  83:  3163 
  • 17 Fu C. Linden A. Heimgartner H. Helv. Chim. Acta  2001,  84:  3319 
  • 18 Zaleska B. Karelus M. Synlett  2002,  1831 
  • 19 Zaleska B. Bazanek T. Socha R. Karelus M. Grochowski J. Serda P. J. Org. Chem.  2002,  67:  2203