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Synthesis 2003(12): 1837-1843
DOI: 10.1055/s-2003-41026
DOI: 10.1055/s-2003-41026
PAPER
© Georg ThiemeVerlag Stuttgart · New York
Syntheses of Showdomycin andits Anomer Using N-(Triisopropylsilyl)pyrrole asa Synthetic Equivalent for the Maleimide C3-Anion
Further Information
Received
9 July 2003
Publication Date:
13 August 2003 (online)
Publication History
Publication Date:
13 August 2003 (online)
Abstract
Showdomycin (1) and its anomer (2) have been prepared in four steps fromreadily available trichloroacetimidate 9.The key step involves reaction of the last compound with the titlepyrrole 3 so as to form a chromatographically separable mixtureof the pyrrole C-glycosides 10 and 11. Thesepyrroles are desilylated then oxidized to the corresponding maleimidesusing PCC.
Key words
nucleosides - pyrroles - trichloroacetimidates - C-glycosides - maleimides - oxidation
- 1
Armitt DJ.Banwell MG.Freeman C.Parish CR. J. Chem. Soc., PerkinTrans. 1 2002, 1743 -
2a
Nishimura H.Mayama M.Komatsu Y.Kato H.Shimsoka N.Tanaka Y. J. Antibiot.,Ser. A 1964, 17: 148 -
2b
Nakagawa Y.Kao H.Tsukuda Y.Koyama H. Tetrahedron Lett. 1967, 4105 -
2c
Darnall KR.Townsend LB.Robins RK. Proc. Natl. Acad. Sci. U.S.A. 1967, 57: 548 -
3a
Yoshihide K.Kentaro T. Agric.Biol. Chem. 1968, 32: 1021 -
3b
Nishimura H.Yoshihide K. J. Antibiot. 1968, 21: 250 -
3c
Roy-Burman S.Huang YH.Visser DW. Biochem. Biophys. Res. Commun. 1971, 42: 445 - 4
Niedzwicki JG.El Kouni MH.Chu SH.Cha S. Biochem. Pharmacol. 1983, 32: 399 -
5a
Roy-Burman P. Recent Results Cancer Res. 1970, 25 -
5b
Vázquez D. Inhibitors of ProteinBiosynthesis Springer Verlag; Berlin: 1979. p.21 -
5c
Megges R.Weiland J.Schön R.Repke H.Repke KRH. Collect.Czech. Chem. Commun. 2002, 67: 336 -
6a
Matsuura S.Shiratori O.Katagiri K. J. Antibiot., Ser. A 1964, 17: 234 -
6b
Rabinovitz M.Uehara Y.Vistica DT. Science 1979, 206: 1085 -
7a
Kalvoda L.Farkas J.Sorm F. Tetrahedron Lett. 1970, 2297 -
7b
Trummlitz G.Moffatt JG. J. Org. Chem. 1973, 38: 1841 -
7c
Kalvoda L. J.Carbohydr. Nucleosides Nucleotides 1976, 3: 47 -
7d
Inoue T.Kuwajima I. J. Chem. Soc., Chem. Commun. 1980, 251 -
7e
Just G.Liak TJ.Lim MJ.Potvin P.Tsantrizos YS. Can.J. Chem. 1980, 58: 2024 -
7f
Kozikowski AP.Ames A. J. Am. Chem.Soc. 1981, 103: 3923 -
7g
Ito Y.Shibata T.Arita M.Sawai H.Ohno M. J.Am. Chem. Soc. 1981, 103: 6739 -
7h
Sato T.Hayakawa Y.Noyori R. Bull.Chem. Soc. Jpn. 1984, 57: 2515 -
7i
Katagiri N.Haneda T.Takahashi N. NucleicAcids Res. 1984, 15: 37 -
7j
Stewart AO.Williams RM. J.Am. Chem. Soc. 1985, 107: 4289 -
7k
Barrett AGM.Broughton HB.Attwood SV.Gunatilaka AAL. J. Org. Chem. 1986, 51: 495 -
7l
Takayama H.Iyobe A.Koizumi T. Chem.Pharm. Bull. 1987, 35: 433 -
7m
Kametani T.Kawamura K.Honda T. J.Am. Chem. Soc. 1987, 109: 3010 -
7n
Gonzalez MSP.Aciego RMD.Herrera FJL. Tetrahedron 1988, 44: 3715 -
7o
Barton DHR.Ramesh M. J.Am. Chem. Soc. 1990, 112: 891 -
7p
Kang SH.Lee SB. TetrahedronLett. 1995, 36: 4089 -
7q
Kang SH.Lee SB. J.Chem. Soc., Chem. Commun. 1995, 1017 -
7r
Trost BM.Kallander LS. J.Org. Chem. 1999, 64: 5427 - 8
Bray BL.Mathies PH.Naef R.Solas DR.Tidwell TT.Artis DR.Muchowski JM. J. Org. Chem. 1990, 55: 6317 -
9a
Watanabe K.Itoh K.Araki Y.Ishido Y. Carbohydr. Res. 1986, 154: 165 -
9b
Chiu-Machado J.Castro-Palomino JC.Madrazo-Alonso O.Loipetegui-Palacios C.Verez-Bencomo V. J. Carbohydr. Chem. 1995, 14: 551 - For related examples of this typeof reaction see
-
10a
Ohoui H.Jones GH.Moffatt JG.Maddox ML.Christensen AT.Byram SK. J.Am. Chem. Soc. 1975, 97: 4602 -
10b
Yokoyama YS.Elmoghayar MRH.Kuwajima I. Tetrahedron Lett. 1982, 23: 2673 - For related examples of this typeof reaction see
-
12a
Casiraghi G.Cornia M.Rassu G.DelSante C.Spanu P. Tetrahedron 1992, 48: 5619 -
12b
Cornia M.Capacchi S.Del Pogetto M.Pelosi G.Fava GG. Tetrahedron:Asymmetry 1997, 8: 2905 - 13
Bernstein MA.Morton HE.Guindon Y. J.Chem. Soc., Perkin Trans. 2 1986, 1155 - 14
Terpin A.Polborn K.Steglich W. Tetrahedron 1995, 51: 9941 - 15
Corey EJ.Suggs JW. Tetrahedron Lett. 1975, 2647 - 16
Tsukuda Y.Koyama H. J. Chem. Soc., B 1970, 1709 - 17
Aslani-Shotorbani G.Buchanan JG.Edgar AR.Shanks CT.Williams GC. J. Chem. Soc., Perkin Trans. 1 1981, 2267 - 18
Dudfield PJ.Le V.-D.Lindell SD.Rees CW. J. Chem. Soc., PerkinTrans. 1 1999, 2929
References
Compound 7 canbe purchased from the Aldrich Chemical Company.