Friedländer reactions of triacetylmethane- unusual distribution of products-

Heterocycles

Volumn 65, Issue 11, 2005, Pages 2777-2782

  Rahman, A F M Motiur ^a   Kwon, Youngjoo ^b   Jahng, Yurngdong ^a  

^a Yeungnam University   (South Korea)

^b Ewha Womans University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33646890414     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-05-10534     Document Type: Article

References (34)

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29. Recent example of base-catalyzed deacetylation. Attanasi O.A., Filippone P., Fiorucci C., Foresti E., and Mantellini F. Strong alkali-catalyzed predeacetylation of 2,4-pentanedione to acetone was also reported, see. J. Org. Chem. 63 (1998) 9880
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33. All reactions were carried out under same reaction conditions. Reaction yields were determined based on the amount of products isolated.
34. 3) δ 8.00 (overlapped dd, J=8.5, 2.0 Hz, 2H, H4 and H8), 7.73 (d, J=8.0 Hz, 1H, H5), 7.65 (ddd, J=8.5, 7.8, 1.4 Hz, 1H, H7), 7.45 (t, J=7.8 Hz, 1H, H6), 7.25 (d, J=9.0 Hz, 1H, H3), 2.72 (s, 3H). Döbner O., and Miller W.v. Ber. 14 (1881) 2816