An Improved Procedure for the Synthesis of Bicyclo[2.2.2]octane-2,6-dione

References

• Hanessian , S. 1983 . ‘Total Synthesis of Natural Products: The Chiron Approach’ , Oxford : Pergamon Press .
   Google Scholar
• Fraser-Reid , B. and Anderson , R. C. 1978 . Fortschr. Chem. Org. Naturst. , 39 : 2
   Google Scholar
• Ho , T.-S. 1992 . ‘Enantioselective synthesis. Natural Products from Chiral Terpenes,’ , New York : John Wiley & Sons .
   Google Scholar
• Coppola , G. M. and Schuster , H. F. 1987 . ‘Asymmetric Synthesis. Construction of Chiral Molecules Using Amino Acids’ , New York : John Wiley & Sons .
   Google Scholar
• Seebach , D. , Imwinkelried , R. and Weber , T. 1986 . Modern Synthetic Methods 1986 , Edited by: Scheffold , R. Vol 4. , 125 – 259 . Springer Verlag .
   Google Scholar
• Helmchen , G. , Karge , R. and Weetman , J. 1986 . Modern Synthetic Methods 1986 , Edited by: Scheffold , R. Vol 4. , 261 – 306 . Springer Verlag .
   Google Scholar
• Mori , K. and Nagano , E. 1990 . Biocatalysis , 3 : 25
   Google Scholar
• Bartlett , P. D. and Woods , G. F. 1940 . J. Am. Chem. Soc. , 62 : 2935
   Google Scholar
• Mori , K. , Nakahara , Y. and Matsui , M. 1972 . Tetrahedron , 28 : 3217
   Web of Science ®Google Scholar
• Gerlach , H. and Möller , W. 1972 . Angew. Chem. , 84 : 1110
   Google Scholar
• Wade , L. G. Jr , Acker , K. J. , Earl , R. A. and Osteryoung , R. A. 1979 . J. Org. Chem. , 44 : 3724
   Web of Science ®Google Scholar
• Chan , C.-C. and Huang , X. 1984 . Synthesis , : 224 Original procedure:
   Google Scholar
• Commercially available or prepared as in Ref 10.
   Google Scholar
• Increasing the amount of acetic acid lowers the yield of 2 and gives more of the UV-active impurity.
   Google Scholar