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  2006(16): 2748-2752  
DOI: 10.1055/s-2006-942500
   DOI: 10.1055/s-2006-942500
PAPER
© Georg Thieme Verlag Stuttgart · New YorkThallium(III)-Mediated Ring Contraction of cis-Octalins: An Approach for the Diastereoselective Construction of the nor-Bakkane Skeleton
Weitere Informationen
            
               
                  
                        
                              Received
                              6 April 2006 
                      
Publikationsdatum:
19. Juli 2006 (online)
            
         
      
   Publikationsverlauf
Publikationsdatum:
19. Juli 2006 (online)

Abstract
A new approach for the diastereoselective synthesis of cis-hydrindanes bearing important structural features of the bakkane skeleton is described. The key step in such a sequence is a thallium trinitrate mediated oxidative rearrangement of cis-octalins. The ring-contraction products thus obtained were elaborated in a diastereoselective fashion into hydrindanes bearing a quaternary center.
Keywords
bakkanes - ring contraction - thallium(III) - hydrindanes - oxidative rearrangement
- 1a 
             
            Abe N.Onoda R.Shirahata K.Kato T.Woods MC.Kitahara Y. Tetrahedron Lett. 1968, 369
- 1b 
             
            Naya K.Takagi I.Hayashi M.Nakamura S.Kobayashi M.Katsumura S. Chem. Ind. (London) 1968, 318
- 2 For a review concerning the chemistry of bakkanes, see:  
            Silva LF. Synthesis 2001, 671
- For examples, see:
- 3a 
             
            Jamieson GR.Reid EH.Turner BP.Jamieson AT. Phytochemistry 1976, 15: 1713
- 3b 
             
            Kano K.Hayashi K.Mitsuhashi H. Chem. Pharm. Bull. 1982, 30: 1198
- 3c 
             
            Wu T.-S.Kao M.-S.Wu P.-L.Lin F.-W.Shi L.-S.Liou M.-J.Li C.-Y. Chem. Pharm. Bull. 1999, 47: 375
- For examples, see:
- 4a 
             
            Nawrot J.Bloszyk E.Harmatha J.Novotný L. J. Appl. Entomol. 1984, 98: 394
- 4b 
             
            Nawrot J.Harmatha J.Novotn L. Biochem. Syst. Ecol. 1984, 12: 99
- 5 
             
            Wu T.-S.Kao M.-S.Wu P.-L.Lin F.-W.Shi L.-S.Teng C.-M. Phytochemistry 1999, 52: 901
- 6 
             
            Liao C.-H.Ko F.-N.Wu T.-S.Teng C.-M. J. Pharm. Pharmacol. 1997, 49: 1248
- 7 
             
            Reddy DS. Org. Lett. 2004, 6: 3345
- 8a 
             
            Back TG.Nava-Salgado VO.Payne JE. J. Org. Chem. 2001, 66: 4361
- 8b 
             
            Back TG.Payne JE. Org. Lett. 1999, 1: 663
- 9a 
             
            Srikrishna A.Reddy TJ. Arkivoc 2001, (viii): 9
- 9b 
             
            Srikrishna A.Nagaraju S.Venkateswarlu S.Hiremath US.Reddy TJ.Venugopalan P. J. Chem. Soc., Perkin Trans. 1 1999, 2069
- 9c 
             
            Hayashi K.Nakamura H.Mitsuhashi H. Chem. Pharm. Bull. 1973, 21: 2806
- 10 
             
            Mori K.Matsushima Y. Synthesis 1995, 845
- 11a 
             
            Evans DA.Sims CL. Tetrahedron Lett. 1973, 4691
- 11b 
             
            Evans DA.Sims CL.Andrews GC. J. Am. Chem. Soc. 1977, 99: 5453
- For some leading references, see:
- 12a 
             
            Brocksom TJ.Coelho F.Depres JP.Greene AE.de Lima MEF.Hamelin O.Hartmann B.Kanazawa AM.Wang YY. J. Am Chem. Soc. 2002, 124: 15313
- 12b 
             
            Hamelin O.Wang Y.Depres JP.Greene AE. Angew. Chem. Int. Ed. 2000, 39: 4314
- 12c 
             
            Hamelin O.Deprés J.-P.Greene AE.Tinant B.Declercq J.-P. J. Am. Chem. Soc. 1996, 118: 9992
- 12d 
             
            Greene AE.Deprés J.-P.Coelho F.Brocksom TJ. J. Org. Chem. 1985, 50: 3943
- 12e  
            For other papers, see, for example: ref. 2 and ref. 12a. 
- 13 
             
            Kabbe H.-J. Justus Liebigs Ann. Chem. 1962, 656: 204
- 14a 
             
            Lee JB.Price MJ. Tetrahedron Lett. 1962, 1155
- 14b 
             
            Lee JB.Price MJ. Tetrahedron 1964, 20: 1017
- 15 
             
            Anderson CB.Winstein S. J. Org. Chem. 1963, 28: 605
- For some reviews concerning thallium(III), see:
- 16a 
             
            McKillop A.Taylor EC. In Comprehensive Organometallic Chemistry Vol. 7:Wilkinson G. Pergamon Press; New York: 1982. p.465
- 16b 
             
            Ferraz HMC.Silva LF.Vieira Tde O. Synthesis 1999, 2001
- 16c 
             
            McKillop A.Taylor EC. In Organic Synthesis by Oxidation with Metal CompoundsMijs WJ.De Jonge CRHI. Plenum; New York: 1986. p.695
- 17a For a review concerning thallium(III)-mediated ring-contraction reactions, see:  
            Ferraz HMC.Silva LF. Quim. Nova 2000, 23: 216
- 17b For a review concerning ring contraction reactions, see:  
            Silva LF. Tetrahedron 2002, 58: 9137
- 18 
             
            Ferraz HMC.Silva LF. Tetrahedron 2001, 57: 9939
- 19 
             
            Ferraz HMC.Silva LF.Vieira TO. Tetrahedron 2001, 57: 1709
- 20 
             
            Silva LF.Sousa RMF.Ferraz HMC.Aguilar AM. J. Braz. Chem. Soc. 2005, 16: 1160
- 21a 
             
            Ferraz HMC.Aguilar AM.Silva LF. Synthesis 2003, 1031
- 21b 
             
            Ferraz HMC.Aguilar AM.Silva LF. Tetrahedron 2003, 59: 5817
- 22 
             
            Ferraz HMC.Silva LF. J. Org. Chem. 1998, 63: 1716
- 23 
             
            Ferraz HMC.Silva LF. J. Braz. Chem. Soc. 2001, 12: 548
- 24 2-Methylcyclohex-2-enone was prepared in two steps (bromination followed by dehydrohalogenation)
            from 2-methylcyclohexanone, in 68% yield:  
            Hua DH.Chen Y.Sin H.-S.Maroto MJ.Robinson PD.Newell SW.Perchellet EM.Ladesich JB.Freeman JA.Perchellet J.-P.Chiang PK. J. Org. Chem. 1997, 62: 6888
- 25 
             
            Nagakura I.Ogata H.Ueno M.Kitahara Y. Bull. Chem. Soc. Jpn. 1975, 48: 2995
- 26 
             
            Fringuelli F.Pizzo F.Taticchi A.Halls TDJ.Wenkert E. J. Org. Chem. 1982, 47: 5056
- 27 
             
            Angell EC.Fringuelli F.Pizzo F.Taticchi A.Wenkert E. J. Org. Chem. 1988, 53: 1224
- 28 
             
            McKillop A.Hunt JD.Kienzle F.Bigham E.Taylor EC. J. Am. Chem. Soc. 1973, 95: 3635
- 29 
             
            Abley P.Byrd JE.Halpern J. J. Am. Chem. Soc. 1973, 95: 2591
- 30 
             
            Sekizaki H.Ito M.Inoue S. Bull. Chem. Soc. Jpn. 1978, 51: 2439
- 31 
             
            Heathcock CH.Ratcliffe R.Van J. J. Org. Chem. 1972, 37: 1796
- 32 
             
            Ratcliffe BE.Heathcock CH. J. Org. Chem. 1972, 37: 531
References
The X-ray data have been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition number CCDC 605577.
 
    