RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2005(3): 437-441
DOI: 10.1055/s-2004-834948
DOI: 10.1055/s-2004-834948
PAPER
© Georg Thieme Verlag Stuttgart · New YorkDirect Halo-Oxygenation of Alkenes with IBX and Potassium Halide
Weitere Informationen
Received
23 August 2004
Publikationsdatum:
03. Dezember 2004 (online)
Publikationsverlauf
Publikationsdatum:
03. Dezember 2004 (online)

Abstract
The direct halo-oxygenation of alkenes by IBX in the presence of potassium halide is described, in which two issues have been approached: (a) the products are formed atom-economically with retention of the main skeleton of IBX; and (b) the products contain multi-functional groups offering further synthetic applicability.
Key words
addition - alkene - halo-oxygenation - hypervalent iodine - IBX
- 1a
Buchmeiser MR. Chem. Rev. 2000, 100: 1565 - 1b
Rodriguez J.Dulcère JP. Synthesis 1993, 1177 - 1c
Chiappe C.Capraro D.Conte V.Pieraccini D. Org. Lett. 2001, 3: 1061 - 1d
Younes MR.Chaabouni MM.Baklouti A. Tetrahedron Lett. 2003, 44: 5263 - 1e
Trofimov BA.Malysheva SF.Sukhov BG.Bdogorlova NA.Schmidt EY.Sobenina LN.Kuimov VA.Gusarova NK. Tetrahedron Lett. 2003, 44: 2629 - 1f
Dahlén A.Hilmersson G. Tetrahedron Lett. 2003, 44: 2661 - 1g
Årstad E.Barrett AGM.Tedeschi L. Tetrahedron Lett. 2003, 44: 2703 - 2a
Zhdankin VV.Stang PJ. Chem. Rev. 2002, 102: 2523 - 2b
Stang PJ.Zhdankin VV. Chem. Rev. 1996, 96: 1123 - 2c
Wirth T.Hirt UH. Synthesis 1999, 1271 - 3
Kirsching A.Plumeier C.Rose L. J. Chem. Soc., Chem. Commun. 1988, 33 - 4
Hashem A.Jung A.Ries M.Kirsching A. Synlett 1998, 195 - 5
Barluenga J.Maro-Arias M.González-Bobes F.Ballesteros A.González J. Chem. Eur. J. 2004, 10: 1677 - 6a
Bruno M.Margarita R.Parlanti L.Piancatelli G.Trifoni M. Tetrahedron Lett. 1998, 39: 3847 - 6b
Margarita R.Mercanti C.Parlanti L.Piancatelli G. Eur. J. Org. Chem. 2000, 1865 - 7
De Mico A.Margarita R.Mariani A.Piancatelli G. Chem. Commun. 1997, 1237 - 8
Tingoli M.Tiecco M.Testaferri L.Temperini A. Synth. Commun. 1998, 28: 1769 - 9
Shi L.Kim YL.Gin DY. J. Am. Chem. Soc. 2001, 123: 6939 - 10
De Mico A.Margarita R.Parlanti L.Piancatelli G.Vescovi A. Tetrahedron 1997, 53: 16877 - 11a
Nicolaou KC.Zhong YL.Baran PS. Angew. Chem. Int. Ed. 2000, 39: 622 - 11b
Nicolaou KC.Baran PS.Zhong YL.Sugita K. J. Am. Chem. Soc. 2002, 124: 2212 - 12a
Nicolaou KC.Baran PS.Zhong YL.Barluenga S.Hunt KW.Kranich R.Vega J. J. Am. Chem. Soc. 2002, 124: 2233 - 12b
Nicolaou KC.Montagnon T.Baran PS.Zhong YL. J. Am. Chem. Soc. 2002, 124: 2245 - 12c
Mülbaier M.Giannis A. Angew. Chem. Int. Ed. 2001, 40: 4393 - 12d
Wirth T. Angew. Chem. Int. Ed. 2001, 40: 2812 - 12e
Frigerio M.Santagostino M. Tetrahedron Lett. 1994, 35: 8019 - 12f
Paintner FF.Allmendinger L.Bauschke G. Synthesis 2001, 2113 - 12g
Legoupy S.Crevisy C.Guillemin JC.Gree R. J. Organomet. Chem. 1998, 567: 75 - 12h
Maiti A.Yadav JS. Synth. Commun. 2001, 31: 1499 - 12i
Bose DS.Srinivas P. Synlett 1998, 977 - 12j
Magdziak D.Rodriguez AA.Van De Water RW.Pettus TRR. Org. Lett. 2002, 4: 285 - 13
Pan ZL.Liu XY.Liang YM. Tetrahedron Lett. 2004, 45: 4101 - 14
Katritzky AR.Duell BL.Gallos JK. Magn. Reson. Chem. 1989, 27: 1007 - 15
Braddock DC.Cansell G.Hermitage S. Synlett 2004, 461