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 2001(5): 0763-0767
DOI: 10.1055/s-2001-12763
DOI: 10.1055/s-2001-12763
PAPER
© Georg Thieme Verlag Stuttgart · New York
Isopropoxy as a Masked Hydroxy Group in Aryl Oxidative Coupling Reactions
Further Information
Received
15 January 2001
Publication Date:
15 October 2004 (online)
Publication History
Publication Date:
15 October 2004 (online)
![](https://www.thieme-connect.de/media/synthesis/200105/lookinside/thumbnails/10.1055-s-2001-12763-1.jpg)
Abstract
Mono- and dihydroxy substituted triphenylenes have been prepared in a one-pot biphenyl/phenyl oxidative coupling reaction, in which isopropoxy acts as a masking/protecting group.
Key words
triphenylene - coupling - radicals - protecting groups - isopropoxy
- 1
Boden N.Bushby RJ.Clements J. J. Chem. Phys. 1993, 98: 5920 -
2a
Markovitsi D.Germain A.Millie P.Lecuyer P.Gallos LK.Argyrakis P.Bengs H.Ringsdorf H. J. Phys. Chem. 1995, 99: 1005 -
2b
Simmerer J.Glusen B.Paulus W.Kettner A.Schuhmacher P.Adam D.Etzbach KH.Siemensmeyer K.Wendorff JH.Ringsdorf H.Haarer D. Adv. Mater. 1996, 8: 815 -
3a
Cooke G.Radhi A.Boden N.Bushby RJ.Lu ZB.Brown SJ.Heath SL. Tetrahedron 2000, 56: 3385 -
3b
Cooke G.Kaushal N.Boden N.Bushby RJ.Lu ZB.Lozman OR. Tetrahedron Lett. 2000, 41: 7955 -
4a
Boden N.Bushby RJ.Cammidge AN.Martin PS. J. Mater. Chem. 1995, 5: 1857 -
4b
Boden N.Bushby RJ.Cammidge AN.El-Mansoury A.Martin PS.Lu ZB. J. Mater. Chem. 1999, 9: 1391. -
5a
Boden N.Bushby RJ.Lu ZB. Liq. Cryst. 1998, 25: 47 -
5b
Boden N.Bushby RJ.Cammidge AN. J. Am. Chem. Soc. 1995, 117: 924 -
5c
Boden N.Bushby RJ.Lu ZB.Eichhorn H. Mol. Cryst. Liq. Cryst. 1999, 332: 2791 -
5d
Boden N.Bushby RJ.Eichhorn H.Lu ZB.Abeysekeara R.Robards AW. Mol. Cryst. Liq. Cryst. 1999, 332: 2803 - 6
Boden N.Bushby R. J.Cammidge A. N.Headdock H. Synthesis 1995, 31 -
7a
Closs F.Haubling L.Henderson P.Ringsdorf H.Schuhmacher P. J. Chem. Soc., Perkin Trans. 1 1995, 829 -
7b
Henderson P.Ringsdorf H.Schuhmacher P. Liq. Cryst. 1995, 18: 191 -
7c
Cooke G.Hell F.Violini S. Synth. Commun. 1997, 27: 3745 - 9
Greene TW.Wuts PGM. Protective Groups in Organic Synthesis 3rd ed. Wiley; New York: 1999. p 924. - 10
Banwell MG.Flynn BL.Steward SG. J. Org. Chem. 1998, 63: 9139 - 11
Boden N.Bushby RJ.Lu ZB.Headdock G. Tetrahedron Lett. 2000, 41: 10117 - 12
Siegman JR.House JJ. J. Org. Chem. 1982, 47: 2773 - 13
Buckley TF.Rapoport H. J. Am. Chem. Soc. 1980, 102: 3056 - 14
Musgrave W. J. Chem. Soc. C. 1971, 1393 - 15
Kobayashi A.Koguchi Y.Kanzaki H.Kajiyama S.Kawazu K. Biosci. Biotechnol. Biochem. 1994, 58: 133
References
Boden N., Bushby R. J., Liu Q. Y., Lozman O. R.; J. Mater. Chem. to be published.