Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2011(15): 2441-2444
DOI: 10.1055/s-0030-1260079
DOI: 10.1055/s-0030-1260079
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Thiophene-Type S,S- and N,S-Ligands Derived from (+)-Nopinone
Further Information
Received
19 April 2011
Publication Date:
21 June 2011 (online)
Publication History
Publication Date:
21 June 2011 (online)
Abstract
The new chiral thiophene 3 was prepared from (+)-nopinone via a de novo construction of the thiophene nucleus. From compound 3 four new S,S- and N,S-ligands, namely the C 1-symmetric 2-(thiophen-2-yl)pyridine 7 and the C 2-symmetric 2,2′-bithiophene 5, 2,6-di(thiophen-2-yl)pyridine 8, and 2,6-di(thiophen-2-yl)thiophene 9 were synthesized.
Key words
thiophene - monoterpenes - (+)-nopinone - coupling reactions - palladium catalysts
-
1a
Wu C.Decker ER.Blok N.Bui H.You TJ.Wang J.Bourgoyne AR.Knowles V.Berens KL.Holland GW.Brock TA.Dixon RAF. J. Med. Chem. 2004, 47: 1969 -
1b
Oberdorf C.Schepmann D.Vela JM.Diaz JL.Holenz J.Wünsch B. J. Med. Chem. 2008, 51: 6531 -
1c
Romagnoli R.Baraldi PG.Carrion MD.Cara CL.Cruz-Lopez O.Iaconinoto MA.Preti D.Shryock JC.Moorman AR.Vincenzi F.Varani K.Borea PA. J. Med. Chem. 2008, 51: 5875 -
1d
Wang WL.Chai SC.Huang M.He HZ.Hurley TD.Ye QZ. J. Med. Chem. 2008, 51: 6110 -
2a
Hwang IT.Kim HR.Jeon DJ.Hong KS.Song JH.Cho KY. J. Agric. Food Chem. 2005, 53: 8639 -
2b
Fokialakis N.Cantrell CL.Duke SO.Skaltsounis AL.Wedge DE. J. Agric. Food Chem. 2006, 54: 1651 - 3
Lamberth C.Jeanguenat A.Cederbaum F.Mesmaeker A.Zeller M.Kempf HJ.Zeun R. Bioorg. Med. Chem. 2008, 16: 1531 -
4a
Yu J.Holdcroft S. Chem. Mater. 2002, 14: 3705 -
4b
Narasimhaswamy T.Somanathan N.Lee DK.Ramamoorthy A. Chem. Mater. 2005, 17: 2013 -
4c
Querner C.Benedetto A.Demadrille A.Rannou P.Reiss P. Chem. Mater. 2006, 18: 4817 -
5a
Barbarella G.Melucci M.Sotgiu G. Adv. Mater. 2005, 17: 1581 -
5b
Melucci M.Barbarella G.Gazzano M.Cavallini M.Biscarini F.Bongini A.Piccinelli F.Monari M.Bandini M.Umani-Ronchi A.Biscarini P. Chem. Eur. J. 2006, 12: 7304 - 6
Dore K.Dubus S.Ho H.-A.Levesque I.Brunette M.Corbeil G.Boissinot M.Boivin G.Bergeron MG.Boudreau D.Leclerc M. J. Am. Chem. Soc. 2004, 126: 4240 - For recent reviews, see:
-
7a
Pellissier H. Chiral Sulfur Ligands: Asymmetric Catalysis Royal Society of Chemistry; Cambridge: 2009. -
7b
Fellah M.Voituriez A.Schulz E. Chem. Rev. 2007, 107: 5133 -
7c
Pellissier H. Tetrahedron 2007, 63: 1297 - For recent examples of chiral ligands containing the thiophene unit, see:
-
7d
Zulauf A.Mellah M.Schulz E. J. Org. Chem. 2009, 74: 2242 -
7e
Zulauf A.Mellah M.Schulz E. Chem. Commun. 2009, 6574 -
7f
Zhang X.-Q.Li Y.-Y.Dong Z.-R.Shen W.-Y.Cheng Z.-B.Gao J.-X. J. Mol. Catal. A: Chem. 2009, 307: 149 -
7g
Zhang XQ.Li YY.Zhang H.Gao JX. Tetrahedron: Asymmetry 2007, 18: 2049 -
8a
Bonini B.-F.Giordano L.Fochi M.Comes-Franchini M.Bernardi L.Capitò E.Ricci A. Tetrahedron: Asymmetry 2004, 15: 1043 -
8b
Macco AA.Buck HM. J. Org. Chem. 1981, 46: 2655 - 9
Smith AJ.Abbott LK.Martin SF. Org. Lett. 2009, 11: 4200 - 10
Majer J.Kwiatkowski P.Jurczak J. Org. Lett. 2009, 11: 4636 -
11a
Bonini C.Chiummiento L.De Bonis M.Funicello M.Lupattelli P.Suanno G.Berti Campaner P. Tetrahedron 2005, 61: 6580 -
11b
Bonini C.Chiummiento L.De Bonis M.Funicello M.Lupattelli P. Tetrahedron Lett. 2004, 45: 2797 -
11c
Crawley GC.Briggs MT. J. Med. Chem. 1995, 38: 3951 - 12
Kanao K.Miyake Y.Nishibayashi Y. Organometallics 2009, 28: 2920 - 13
Tamao K.Nakamura K.Ishii H.Yamaguchi S.Shiro M. J. Am. Chem. Soc. 1996, 118: 12469 -
14a
Grimshaw N.Grimshaw JT.Juneja HR. J. Chem. Soc., Perkin Trans. 1 1972, 50 -
14b
Brown HC.Weissman SA.Perumal PT.Dhokte UP. J. Org. Chem. 1990, 55: 1217 - 15
Waldvogel E. Helv. Chim. Acta 1992, 75: 907 - 16
Zhu SS.Swager TM. J. Am. Chem. Soc. 1997, 119: 12568 - 17
Miller LL.Yu Y. J. Org. Chem. 1995, 60: 6813