Journal of Organic Chemistry p. 1972 - 1979 (1987)
Update date:2022-07-29
Topics:
Schuda, Paul Francis
Price, William A.
The Friedel-Crafts acylation reaction was studied on several acid-sensitive substrates.Under the proper conditions of varying Lewis acids, solvents, and reaction temperatures, the acylation indeed took place, thus obviating the necessity for functional group protection-deprotection sequences.By use of these procedures, the naturally occuring isoflavones jamaicin (1), calopogonium isoflavone-B (2), maxima substance-B (30), and pseudobaptigenin (31) were synthesized and characterized.
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Doi:10.1039/b808638a
(2008)Doi:10.1002/jlcr.3079
(2013)Doi:10.1021/ja00245a030
(1987)Doi:10.1016/S0022-2860(00)00521-4
(2000)Doi:10.1002/anie.201208305
(2013)Doi:10.1055/s-1986-31734
(1986)