References
- Adlington , R. M. , Baldwin , J. E. , Catterick , D. and Pritchard , G. J. 1999 . J. Chem. Soc., Perkin Trans. , 1 : 855
- Adlington , R. M. , Baldwin , J. E. , Catterick , D. and Pritchard , G. J. 1997 . Chem. Commun. , : 1757
- Chauvelier , J. 1954 . Bull. Soc. Chim. Fr. , : 272
- Sparks , W. J and Marvel , C. S. 1936 . J. Am. Chem. Soc. , 58 : 865
- Burgstahler , A. W. and Widiger , G. N. 1973 . J. Org. Chem. , 38 : 3652
- Hauptmann , H. 1976 . Tetrahedron , 32 : 1293
- Sisido , K. , Hirowatari , N. , Tamura , H. , Kobata , H. , Takagisi , H. and Isida , Y. 1970 . J. Org. Chem. , 35 : 350
- Rule , N. G. , Detty , M. R. , Kaeding , J. E. and Sinicropi , J. A. 1995 . J. Org. Chem. , 60 : 1665
- Wadsworth , D. H. , Greer , S. M. and Detty , M. R. 1987 . J. Org. Chem. , 52 : 3662
- van Amsterdam , L. J.P. and Lughenburg , J. 1982 . J. Chem. Soc., Chem. Commun. , : 946
- Ito , Y. , Inouye , M. and Murakami , M. 1989 . Chem. Lett. , : 1261
- Midland , M. M. , Tramontano , A. and Cable , J. R. 1980 . J. Org. Chem. , 45 : 28 Midland has successfully used lithio ethyl propiolate to add to aldehydes and ketones
- Logue , M. W. and Teng , K. 1982 . J. Org. Chem. , 47 : 2549
- Normant , J. F. 1972 . Synthesis , : 63
- Logue , M. W. and Moore , G. L. 1975 . J. Org. Chem. , 40 : 131
- Boche , G. and Bigalke , J. 1984 . Tetrahedron Lett. , 25 : 955
- Durand , M. H. 1961 . Bull. Soc. Chim. Fr. , : 2387 The alkyl aldehydes are supplied from the Lancaster Chemical Company as their diethyl acetals. The aldehydes can be liberated using a procedure reported by Durand
- Caprino , L. A. 1970 . J. Org. Chem. , 35 : 3971
- Just , G. , Luthe , C. and Viet , M. T.P. 1983 . Can. J. Chem. , 61 : 712
- Shattuck , J. C. , Svatoš , A. , Blazey , C. M. and Meinwold , J. 1997 . Tetrahedron Lett. , 38 : 6803
- Hlasta , D. J. and Court , J. J. 1989 . Tetrahedron Lett. , 30 : 1773 This reagent has also been independently developed by Hlasta and Court
- Whipple , W. L. and Reich , H. J. 1991 . J. Org. Chem. , 56 : 2912
- We have found that compound 10 rapidly decomposes when left for periods greater than 90 minutes
- Meerwein , H. , Borner , P. , Fuchs , O. , Sasse , H. J. , Schrodt , H. and Spille , J. 1956 . Chem. Ber. , 89 : 2060 Triethoxycarbenium tetrafluoroborate is prepared by the alkylation of diethyl carbonate with triethyloxonium tetrafluoroborate