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 2006(12): 2053-2063
DOI: 10.1055/s-2006-942372
DOI: 10.1055/s-2006-942372
PAPER
© Georg Thieme Verlag Stuttgart · New YorkA Concise Synthesis of Pyrrolo- and Pyrrolidino[1,2-a]quinolin-1-ones via Diels-Alder Reactions of N-Acyliminium Cations with Olefins
Further Information
Received
12 December 2005
Publication Date:
05 May 2006 (online)
Publication History
Publication Date:
05 May 2006 (online)

Abstract
A concise and efficient synthesis of pyrrolo- and pyrrolidino[1,2-a]quinolin-1-ones has been developed. New members of this family can thus be generated via Diels-Alder reactions of olefins with N-acyliminium cations produced, in the presence of BF3·Et2O, from 5-hydroxy-1-arylpyrrol-2-ones and 5-hydroxy-1-arylpyrrolidin-2-ones in moderate to high yields at ambient temperature.
Key Words
N-acyliminium cation - Diels-Alder reaction - alkenes - 5-hydroxy-1-arylpyrrol-2-one - pyrrolo[1,2-a]quinolin-1-one
- 1
Anderson WK.Heider AR.Raiu N.Yucht JA. J. Med. Chem. 1988, 31: 2096 - 2
Ager IR.Barnes AC.Danswan GW.Hairsine PW.Kay DP.Kennewell PD.Matharu SS.Miller P.Robson P. J. Med. Chem. 1988, 31: 1098 - 3a
Michael JP.de Koning CB.Stanbury TV. Tetrahedron Lett. 1996, 52: 9403 - 3b
Chu DTW.Lico IM.Claiborne AK.Plattner JJ.Pernet AG. Drugs Exp. Clin. Res. 1990, 16: 215 - 3c
Glushkov RG.Marchenco NB.Padeiskaya EN.Shipilova LD. Khim.-Farm. Zh. 1990, 24: 24 - 3d
Bertram HJ,Fischer R,Hagmann H,Krueger BW,Schenke T, andErdelen G. inventors; Ger. Offen. DE 4032090. ; Chem. Abstr. 1991, 115, 232069a - 4
Ishihara Y.Kiyota Y.Goto G. Chem. Pharm. Bull. 1990, 38: 3024 - 5a
Wei L.Hsung RP.Sklenicka HM.Gerasyuto AI. Angew. Chem. Int. Ed. 2001, 40: 1516 - 5b
Pearson WH.Fang W. J. Org. Chem. 2000, 65: 7158 - 5c
Pearson WH.Fang W. J. Org. Chem. 2001, 66: 6838 - 5d
Hart DJ.Kanai K. J. Am. Chem. Soc. 1983, 105: 1255 - 5e
Ito Y.Nakajo E.Nakatsuka M.Saegusa T. Tetrahedron Lett. 1983, 24: 2881 - 5f
Fujimoto R.Kishi Y.Blount JF. J. Am. Chem. Soc. 1980, 102: 7154 - 6a
Lang S.Kennedy AR.Murphy JA.Payne AH. Org. Lett. 2003, 5: 3655 - 6b
Deady LW.Werden DM. J. Org. Chem. 1987, 52: 3930 - 6c
Eicher T.Rohde R. Synthesis 1985, 619 - 6d
Yakushijin K.Tsuruta T.Furukawa H. Chem. Pharm. Bull. 1982, 30: 140 - 7a
Maryanoff BE.Zhang H.-C.Cohen JH.Turchi IJ.Maryanoff CA. Chem. Rev. 2004, 104: 1431 - 7b
Royer J.Bonin M.Micouin L. Chem. Rev. 2004, 104: 2311 - 7c
Speckamp WN.Hiemstra H. Tetrahedron 1985, 41: 4367 - 8a
He F.Bo Y.Altom JD.Corey EJ. J. Am. Chem. Soc. 1999, 121: 6771 - 8b
Hiemstra H.Speckamp WN. In The Alkaloids Vol. 32:Brossi A. Academic Press; New York: 1988. p.271 - 8c
Hiemstra H.Speckamp WN. In Comprehensive Organic Synthesis Vol. 2:Trost BM.Fleming I. Pergamon; Oxford: 1991. p.1047-1082 - 8d
Hart DJ. Alkaloids, Chemical and Biological Perspectives Vol. 6:Pelletier SW. Wiley; New York: 1988. p.227 - 9a
Pigeon P.Othman M.Netchitailo P.Decroix B. J. Heterocycl. Chem. 1999, 36: 691 - 9b
Pigeon P.Decroix B. Synth. Commun. 1998, 28: 2507 - 10a
Zhang W.Guo Y.Liu Z.Jin X.Yang L.Liu ZL. Tetrahedron 2005, 43: 9433 - 10b
Huo C.Wei R.Zhang W.Yang L.Lu J.Liu ZL. Synlett 2005, 161 - 10c
Huo C.Jia X.Zhang W.Yang L.Lu J.Liu ZL. Synlett 2004, 251 - 10d
Zhang W.Jia X.Yang L.Liu ZL. Tetrahedron Lett. 2002, 43: 9433 - 10e
Jia X.Lin H.Huo C.Zhang W.Lu J.Yang L.Liu ZL. Synlett 2003, 1707 - 10f
Zhang W.Shao X.Yang L.Liu ZL.Chow YL. J. Chem. Soc., Perkin Trans. 2 2002, 1029 - 11a
Mase N.Nishi T.Hiyoshi M.Ichihara K.Bessho J.Yoda H.Takabe K. J. Chem. Soc., Perkin Trans. 1 2002, 707 - 11b
Hubert JC.Wijnberg JBPA.Speckamp WN. Tetrahedron Lett. 1975, 31: 1437