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  2005(7): 1087-1094  
DOI: 10.1055/s-2005-861862
   DOI: 10.1055/s-2005-861862
PAPER
© Georg Thieme Verlag Stuttgart · New YorkStereoselective Synthesis of (1R,5S)-4-[(E)-Alkylidene]-1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-ones
Further Information
            
               
                  
                        
                              Received
                              3 November 2004 
                      
Publication Date:
09 March 2005 (online)
            
         
      
   Publication History
Publication Date:
09 March 2005 (online)

Abstract
Various (1R,5S)-4-[(E)-alkylidene]-1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-ones were prepared, stereoselectively, via coupling of (1R,5S)-4-[(E)-(dimethylamino)methylidene]-1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-one with Grignard reagents, potassium cyanide, and 2-methyl-1H-indole.
Key words
Grignard reactions - chiral pool - coupling - terpenoids - enaminones
- 1a 
             
            Money T. Nat. Prod. Rep. 1985, 253
- 1b 
             
            Oppolzer W. Tetrahedron 1987, 43: 1969
- 1c 
             
            Oppolzer W. Pure Appl. Chem. 1990, 62: 1241
- 1d 
             
            Money T. Remote Functionalization of Camphor: Application to Natural Product Synthesis in Organic Synthesis: Theory and Applications Vol 3: JAI Press Inc.; Greenwich, London: 1996. p.1
- For recent reviews see:
- 2a 
             
            Stanovnik B.Svete J. Synlett 2000, 1077
- 2b 
             
            Stanovnik B.Svete J. In Targets in Heterocyclic Systems Vol. 4: Italian Society of Chemistry; Roma: 2000. p.105
- 2c 
             
            Svete J. J. Heterocycl. Chem. 2002, 39: 437
- 2d 
             
            Svete J. Monatsh. Chem. 2004, 135: 629
- 2e 
             
            Stanovnik B.Svete J. Chem. Rev. 2004, 104: 2433
- 3a 
             
            Pirc S.Bevk D.Golič Grdadolnik S.Svete J. ARKIVOC 2003, Part xiv: 37
- 3b 
             
            Westman J.Lundin R. Synthesis 2003, 1025
- 3c 
             
            Čebaek P.Wagger J.Bevk D.Jakše R.Svete J.Stanovnik B. J. Comb. Chem. 2004, 6: 356
- 4 
             
            Benary E. Chem. Ber. 1931, 64: 2543
- 5a 
             
            Ziegler FE.Guenther T.Nelson RV. Synth. Commun. 1980, 10: 661
- 5b 
             
            Asokan CV.Balu MP.Ila H.Junjappa H. Synthesis 1988, 727
- 5c 
             
            Hutchinson JH.Money T. Tetrahedron Lett. 1985, 26: 1819
- 5d 
             
            Moody CM.Young DW. J. Chem. Soc., Perkin Trans. 1 1997, 3519
- 6a 
             
            Abdulla RF.Fuhr KH. J. Org. Chem. 1978, 43: 4248
- 6b 
             
            Sanin AV.Nenajdenko VG.Smolko KI.Denisenko DI.Balenkova ES. Synthesis 1998, 842
- 7 
             
            Grošelj U.Rečnik S.Svete J.Meden A.Stanovnik B. Tetrahedron: Asymmetry 2002, 13: 821
- 8 
             
            Grošelj U.Bevk D.Jakše R.Meden T.Pirc S.Rečnik S.Stanovnik B.Svete J. Tetrahedron: Asymmetry 2004, 15: 2367
- 9a 
             
            Titman JJ.Foote J.Jarvis J.Keeler J.Neuhaus D. J. Chem. Soc., Chem. Commun. 1991, 419
- 9b 
             
            Ando T.Koseki N.Toia RF.Casida JE. Magn. Res. Chem. 1993, 31: 90
- 9c 
             
            Fischer P.Schweizer E.Langner J.Schmidt U. Magn. Res. Chem. 1994, 32: 567
- 10a 
             
            Golič-Grdadolnik S.Stanovnik B. Magn. Res. Chem. 1997, 35: 482
- 10b 
             
            kof M.Svete J.Stanovnik B.Golič L.Golič-Grdadolnik S.Selič L. Helv. Chim. Acta 1998, 81: 2332
- 10c 
             
            Ba J.Rečnik S.Svete J.Golič-Grdadolnik S.Stanovnik B. ARKIVOC 2001, Part ii: 61
- 10d 
             
            Bevk D.Kmetič M.Rečnik S.Svete J.Golič L.Golobič A.Stanovnik B. Chem. Heterocycl. Compd. 2001, 1651
- 10e 
             
            Jakše R.Rečnik S.Svete J.Golobič A.Golič L.Stanovnik B. Tetrahedron 2001, 57: 8395
- 10f 
             
            Jakše R.Kroelj V.Rečnik S.Sorak G.Svete J.Stanovnik B.Golič-Grdadolnik S. Z. Naturforsch., B: Chem. Sci. 2002, 57: 453
- 10g 
             
            Pirc S.Rečnik S.kof M.Svete J.Golič L.Meden A.Stanovnik B. J. Heterocycl. Chem. 2002, 39: 411
- 11 
             Collect Software  
            Nonius BV; 
            Delft, The Netherlands: 
            1998. 
            
            
            Reference Ris Wihthout Link
- 12 
             
            Otwinowski Z.Minor W. Methods Enzymol. 1997, 276: 307
- 13 
             
            Altomare A.Burla MC.Camalli M.Cascarano GL.Giacovazzo C.Guagliardi A.Moliterni AGG.Polidori G.Spagna R. J. Appl. Cryst. 1999, 32: 115
- 14 
             
            Hall SR.King GSD.Stewart JM. The Xtal 3.4 User"s Manual University of Western Australia; Lamb, Perth: 1995.Reference Ris Wihthout Link
- 15 
             
            Burnett MN.Johnson CK. ORTEP-III: Oak Ridge Thermal Ellipsoid Plot Program for Crystal Structure Illustrations Oak Ridge National Laboratory Report; USA: 1996. p.ORNL-6895Reference Ris Wihthout Link
- 16 
             
            Wang H.Robertson BE. Structure and Statistics in CrystallographyWilson AJC. Adenine Press; New York: 1985.Reference Ris Wihthout Link
References
Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 254265-254268. Copies of the data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html.
 
    