RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2008(2): 197-200
DOI: 10.1055/s-2007-1000861
DOI: 10.1055/s-2007-1000861
PAPER
© Georg Thieme Verlag Stuttgart · New York
Expeditious and Practical Synthesis of Various Substituted Taurines from Amino Alcohols
Weitere Informationen
Received
3 October 2007
Publikationsdatum:
18. Dezember 2007 (online)
Publikationsverlauf
Publikationsdatum:
18. Dezember 2007 (online)
Abstract
Various substituted taurines have been synthesized expeditiously and practically in satisfactory to good yields directly from amino alcohols using a two-step, one-pot procedure, in which the amino alcohols undergo sulfuric acid esterification and subsequent sodium sulfite substitution. Treatment of amino-substituted secondary alcohols using the same procedure gave 2-substituted or 1,2-disubstituted taurines, indicating the formation of aziridines as intermediates during the substitution step. This method is one of the most efficient routes for preparing structurally diverse 2-substituted and 1,2- and 2,2-disubstituted taurines.
Key words
amino acids - aminoalkanesulfonic acids - amino alcohols - sulfates - taurines
- 1 For a review, see:
Xu JX. Chin. J. Org. Chem. 2003, 23: 1 - 2 For a review, see:
Timothy C.Birdsall ND. Alt. Med. Rev. 1998, 3: 128 - 3
Wickberg B. Acta Chem. Scand. 1957, 11: 506 - 4 For a review, see:
Huxtable RJ. Physiol. Rev. 1992, 72: 101 -
5a
Sinnecker S.Svensen N.Barr EW.Ye S.Bollinger JM.Neese F.Krebs C. J. Am. Chem. Soc. 2007, 129: 6168 -
5b
Guz G.Oz E.Lortlar N.Ulusu NN.Nurlu N.Demirogullari B.Omeroglu S.Sert S.Karasu C. Amino Acids 2007, 32: 405 -
5c
Giordano C.Lucente G.Masi A.Paradisi MP.Sansonea A.Spisani S. Bioorg. Med. Chem. 2006, 14: 2642 - 6
Gold MH.Skebelsky M.Lang G. J. Org. Chem. 1951, 16: 1500 -
7a
Higashiura H.Morino H.Matsuura H.Toyomaki Y.Ienaga K. J. Chem. Soc., Perkin Trans. 1 1989, 1479 -
7b
Braghiroli D.Di Bella M. Tetrahedron: Asymmetry 1996, 7: 2145 -
8a
Higashiura K.Ienaga K. J. Org. Chem. 1992, 57: 764 -
8b
Moree WJ.van der Marel GA.Liskamp RMJ. Tetrahedron Lett. 1992, 33: 6389 -
8c
Moree WJ.van der Marel GA.Liskamp RMJ. J. Org. Chem. 1995, 60: 5157 -
8d
Monnee MCF.Marijne MF.Brouwer AJ.Liskamp RMJ. Tetrahedron Lett. 2000, 41: 7991 -
9a
Braghiroli D.Mussati E.Di Bella M.Saladini M. Tetrahedron: Asymmetry 1996, 7: 831 -
9b
Braghiroli D.Di Bella M. Tetrahedron Lett. 1996, 37: 7319 -
10a
Brouwer AJ.Monnee MCF.Liskamp RMJ. Synthesis 2000, 1579 -
10b
Lowik DWPM.Liskamp RMJ. Eur. J. Org. Chem. 2000, 1219 -
10c
Xu JX.Xu S. Synthesis 2004, 276 -
10d
Xu JX.Xu S.Zhang QH. Heteroat. Chem. 2005, 16: 466 - 11
Wang BY.Zhang W.Zhang LL.Du D.-M.Liu G.Xu JX. Eur. J. Org. Chem. 2008, DOI: 10.1002/ejoc.200700791 - 12
Cordero FM.Cacciarini M.Machetti F.De Sarlo F. Eur. J. Org. Chem. 2002, 1407 - 13
Huang JX.Wang F.Du D.-M.Xu JX. Synthesis 2005, 2122 - 14
Huang JX.Du D.-M.Xu JX. Synthesis 2006, 315 - 15
Xu JX. Tetrahedron: Asymmetry 2002, 13: 1129 - 16
Hu LB.Zhu H.Du D.-M.Xu JX. J. Org. Chem. 2007, 72: 4543 -
17a
Rumpf P. Bull. Soc. Chim. Fr. 1955, 945 -
17b
Kanetani F.Tanaka T.Nakano S.Negoro K. Nippon Kagaku Kaishi 1982, 824 -
17c
Senoo A.Enomoto T.Nagata T. Jpn. Kokai Tokkyo Koho 1995, 5 ; Chem. Abstr. 1995, 123, 285232 -
18a
Wenker H. J. Am. Chem. Soc. 1935, 57: 2328 -
18b
Leighton PA.Perkins WA.Renquist MI. J. Am. Chem. Soc. 1947, 69: 1540 - 19
Ma LG.Xu JX. Prog. Chem. 2004, 16: 220 - 20
McKennon M.Meyers AI.Drauz K.Schwarm M. J. Org. Chem. 1993, 58: 3568 - 21
Steiger RE. Org. Synth. 1944, 24: 9