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-00000083.xml
Synlett 2003(9): 1299-1302
DOI: 10.1055/s-2003-40327
DOI: 10.1055/s-2003-40327
LETTER
© Georg Thieme Verlag Stuttgart ˙ New York
Cascade 4+1 Radical Annulations of 2,6-Disubstituted Phenyl Isonitriles with N-Propargyl-6-Iodopyridones: Scope, Mechanism and Regioselective Synthesis of 7,9-Disubstituted Camptothecin Analogs
Further Information
Received
20 February 2003
Publication Date:
30 June 2003 (online)
Publication History
Publication Date:
30 June 2003 (online)
Abstract
The reaction of o,o′-dialkyl-substituted aryl isonitriles with N-propargyl-6-iodopyridones provides 11H-indolizino[1,2-b]quinolin-9-ones with significant regioselectivity in favor of the more crowded product. The usefulness of the method is illustrated with a regioselective synthesis of (20S)-7-trimethylsilyl-9-isopropyl camptothecin.
Key words
cascade radical annulation - isonitrile - camptothecin - mappicine - quinoline
-
1a
Lerchen H.-G. Drugs Fut. 2002, 29: 869 -
1b
Zunino F.Dallavalle S.Laccabue D.Beretta G.Merlini L.Pratesi G. Curr. Pharm. Design 2002, 8: 2505 -
1c
Kim D.-K.Lee N. Mini Rev. Med. Chem. 2002, 2: 611 -
2a
Pirillo A.Verotta L.Gariboldi P.Torregiani E.Bombardelli E. J. Chem. Soc., Perkin Trans. 1 1995, 583 -
2b
Pendrak I.Barney S.Wittrock R.Lambert DM.Kingsbury WD. J. Org. Chem. 1994, 59: 2623 -
2c
Pendrak I.Wittrock R.Kingsbury WD. J. Org. Chem. 1995, 60: 2912 -
2d
Boger DL.Hong JY. J. Am. Chem. Soc. 1998, 120: 1218 -
3a
Curran DP.Liu H. J. Am. Chem. Soc. 1991, 113: 2127 -
3b
Curran DP.Ko SB.Josien H. Angew. Chem., Int. Ed. Engl. 1995, 34: 2683 -
3c
Curran DP.Liu H.Josien H.Ko SB. Tetrahedron 1996, 52: 11385 -
3d
Josien H.Curran DP. Tetrahedron 1997, 53: 8881 -
3e
Josien H.Ko SB.Bom D.Curran DP. Chem.-Eur. J. 1998, 4: 67 -
3f
Zhang Q.Rivkin A.Curran DP. J. Am. Chem. Soc. 2002, 124: 5774 -
4a
Ryu I.Sonoda N.Curran DP. Chem. Rev. 1996, 96: 177 -
4b
Nanni D. In Radicals in Organic Synthesis Vol. 2, 1st ed.:Renaud P.Sibi MP. Wiley-VCH; Weinheim: 2001. p.44-61 -
5a
Curran DP.Josien H.Bom D.Gabarda A.Du W. In The Camptothecins: Unfolding their Anticancer Potential Vol. 922:Liehr JG.Giovanella BC.Verschraegen CF. NY Acad. Sci.; NY: 2000. p.112-21 -
5b
Josien H.Bom D.Curran DP.Zheng Y.-H.Chou T.-C. Bioorg. Med. Chem. Lett. 1997, 7: 3189 -
5c
Bom D.Du W.Garbarda A.Curran DP.Chavan AJ.Kruszewski S.Zimmer SG.Fraley KA.Bingcang AL.Wallace VP.Tromberg BJ.Burke TG. Clinical Cancer Research 1999, 5: 560 -
5d
Bom D.Curran DP.Kruszewski S.Zimmer SG.Thompson Strode J.Kohlhagen G.Du W.Chavan AJ.Fraley KA.Bingcang AL.Latus LJ.Pommier Y.Burke TG. J. Med. Chem. 2000, 43: 3970 -
5e
de Frutos O.Curran DP. J. Comb. Chem. 2000, 2: 639 -
5f
Luo ZY.Zhang QS.Oderaotoshi Y.Curran DP. Science 2001, 291: 1766 -
5g
Gabarda AE.Du W.Isarno T.Tangirala RS.Curran DP. Tetrahedron 2002, 58: 6329 -
5h
Gabarda AE. PhD Thesis University of Pittsburgh; USA: 2002. - 7 A single example of a reaction
with a disubstituted isonitrile has been described previously. See
ref. and:
Liu H. PhD Thesis University of Pittsburgh; USA: 1991. - Fragmentation reactions of cyclohexadienyl-like radicals with rearomatization are well precedented. See, for example:
-
8a
Binmore G.Walton JC.Cardellini L. J. Chem. Soc., Chem. Commun. 1995, 27 -
8b
Jackson L.Walton JC. Tetrahedron Lett. 1999, 40: 7019 -
8c
Jackson LV.Walton JC. Chem. Commun. 2000, 2327
References
Camptothecin numbering and ring designations are used for consistency throughout the manuscript.
9Supporting Information Available: A print or pdf file of the characterization data for the compounds in this paper can be obtained on request from DPC.