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-00000083.xml
Synlett 2011(10): 1449-1453
DOI: 10.1055/s-0030-1260562
DOI: 10.1055/s-0030-1260562
LETTER
© Georg Thieme Verlag
Stuttgart ˙ New York
Regioselectivity in Thermal Rhodium(II)-Catalysed Büchner-Type Reactions of Substituted Aryl Halides: Studies towards the Synthesis of Halide-Substituted Cycloheptatrienes
Weitere Informationen
Received
23 March 2011
Publikationsdatum:
13. Mai 2011 (online)
Publikationsverlauf
Publikationsdatum:
13. Mai 2011 (online)
Abstract
The results of Büchner-type reactions of various substituted aryl halide derivatives with ethyl diazoacetate are presented, together with a discussion of factors affecting the regioselectivity of these processes.
Key words
Büchner reaction - regioselectivity - cycloaddition - carbenoids - rearrangement
- Supporting Information for this article is available online:
- Supporting Information
-
1a
Doyle MP.McKervey MA.Ye T. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds Wiley-Interscience; New York: 1998. -
1b
Ye T.Mckervey MA. Chem. Rev. 1994, 94: 1091 -
2a
Anciaux AJ.Demonceau A.Hubert AJ.Noels AF.Petiniot N.Teyssie P. J. Chem. Soc., Chem. Commun. 1980, 16: 765 -
2b
Anciaux AJ.Demonceau A.Noels AF.Hubert AJ.Warin R.Teyssie P. J. Org. Chem. 1981, 46: 873 -
3a
Kürtz L.Czakó B. Strategic Applications of Named Reactions in Organic Synthesis Elsevier Academic Press; Amsterdam: 2005. -
3b
Maguire AR.Buckley NR.O’Leary P.Ferguson G. J. Chem. Soc., Perkin Trans. 1 1998, 24: 4077 -
3c
Maguire AR.Buckley NR.O’Leary P.Ferguson G. Chem. Commun. 1996, 22: 2595 -
3d
Kane JL.Shea KM.Crombie AL.Danheiser RL. Org. Lett. 2001, 3: 1081 -
3e
Frey B.Wells AP.Rogers DH.Mander LN. J. Am. Chem. Soc. 1998, 120: 1914 - See ref. 2a and 2b. See also:
-
4a
Lovely CJ.Browning RG.Badarinarayana V.Dias HVR. Tetrahedron Lett. 2005, 46: 2453 -
4b
Morilla ME.Diaz-Requejo MM.Belderrain TR.Nicasio MC.Trofimenko S.Perez PJ. Organometallics 2004, 23: 293 - 5 See ref. 1a, 2a, and 2b. See also:
Gale DM. J. Org. Chem. 1968, 33: 2536 - For the discovery of the antibacterial agent emmacin, see:
-
6a
Wyatt EE.Fergus S.Galloway WRJD.Bender A.Fox DJ.Plowright AT.Jessiman AS.Welch M.Spring DR. Chem. Commun. 2006, 3296 -
6b
Wyatt EE.Fergus S.Galloway WRJD.Bender A.Thomas GL.Welch M.Loiseleur O.Plowright AT.Spring DR. Chem. Commun. 2008, 4962 - For recent reviews on DOS, see:
-
6c
Schreiber SL. Nature (London) 2009, 457: 153 -
6d
Galloway WRJD.Isidro-Llobet A.Spring DR. Nat. Commun. 2010, 1: 80 -
6e
Nielsen E.Schreiber SL. Angew. Chem. Int. Ed. 2008, 47: 48 -
6f
Galloway WRJD.Bender A.Welch M.Spring DR. Chem. Commun. 2009, 2446 -
6g
Cordier C.Morton D.Murrison S.Nelson A.O’Leary-Steele C. Nat. Prod. Rep. 2008, 25: 719
References and Notes
A full account of our computational modelling studies on the Büchner reactions described in this paper will be reported in due course.