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 2003(10): 1569-1573
DOI: 10.1055/s-2003-40511
DOI: 10.1055/s-2003-40511
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York
Poly(ethylene glycol) Supported Liquid-Phase Synthesis of 1,2,4-Oxadiazolines
Further Information
Received
24 March 2003
Publication Date:
08 July 2003 (online)
Publication History
Publication Date:
08 July 2003 (online)
Abstract
The liquid-phase synthesis of oxadiazolines via 1,3-dipolar cycloaddition reaction on poly(ethylene glycol) support (PEG) is described. 1,3-Dipolar cycloadditions of nitrile oxide generated in situ on soluble polymer with a variety of imines provided a library of 1,2,4-oxadiazolines in good yields and purity. The reactions were run in the homogeneous phase and the synthetic sequences were performed in parallel one-pot fashion. Quantitative conversion in the 1,3-dipolar cycloaddition reaction was verified by 1H NMR analysis. The polymer bound products were isolated in excellent yields by simple precipitation of the soluble support.
Key words
1,3-dipolar cycloaddition - soluble polymer - liquid-phase synthesis - oxadiazolines - poly(ethylene glycol)
-
1a
Früchtel JS.Jung G. Angew. Chem., Int. Ed Engl.. 1996, 35: 17 -
1b
Allin SM.Sharma PK. Synthesis 1997, 1217 -
1c
Ellmann JA. Chem. Rev. 1996, 96: 555 -
1d
Krch V.ák Holladay MW. Chem. Rev. 2002, 102: 61 - 2
Nefzi A.Otresh JM.Houghten RA. Chem. Rev. 1997, 97: 449 -
3a
Gravert DJ.Janda KD. Chem. Rev. 1997, 97: 489 -
3b
Wentworth P.Janda KD. Chem. Commun. 1999, 1917 -
3c
Toy PH.Tanda KD. Acc. Chem. Res. 2000, 33: 546 -
4a
Yeh CM.Tung CL.Sun CM. J. Comb. Chem. 2000, 2: 341 -
4b
Zhao X.Metz WA.Sieber F.Janda KD. Tetrahedron Lett. 1998, 39: 8433 -
4c
Blettner CG.Konig WA.Quhter G.Stenzel W.Schotten T. Synlett 1999, 307 -
4d
Luisa G.Giorgio M.Pietro C. J. Chem. Soc., Perkin Trans. 1 2002, 2504 -
4e
Racker R.Doring K.Reiser O. J. Org. Chem. 2000, 65: 6932 -
4f
Annunziata R.Benaglia M.Cinquini M.Cozzi F. Chem.-Eur. J. 2000, 6: 133 - 5
Chimirri A.Grasso S.Monforte AM.Monforte P.Zappala M.Carotti A. Chem. Pharm. Bull. 1980, 28: 3296 -
6a
Lenaers R.Eloy F. Helv. Chim. Acta 1963, 46: 1067 -
6b
Morocchi S.Ricca A.Velo L. Chim. Ind. 1967, 49: 168 -
6c
Enders D.Meyer I.Runsink J.Raabe G. Heterocycles 1999, 50: 995 -
7a
Shang YJ.Wang YG. Tetrahedron Lett. 2002, 43: 2247 -
7b
Xia M.Wang YG. Tetrahedron Lett. 2002, 43: 7703 -
7c
Shang YJ.Wang YG. Synthesis 2002, 1663 -
7d
Lin XF.Ma C.Yang YW.Wang YG. Chin. Chem. Lett. 2002, 13: 705 ; Chem. Abstr. 2003, 138, 137115 - 8
Maurizio B.Mauro C.Franco C. Tetrahedron Lett. 1999, 40: 2019