Synthesis and structural revision of naturally occurring ayapin derivatives

被引:50
作者
Maes, D
Vervisch, S
Debenedetti, S
Davio, C
Mangelinckx, S
Giubellina, N
De Kimpe, N
机构
[1] Univ Ghent, Dept Organ Chem, Fac Biosci Engn, B-9000 Ghent, Belgium
[2] Natl Univ La Plata, Dept Biol Sci, Fac Sci, RA-1900 La Plata, Argentina
[3] Univ Buenos Aires, Fac Farm & Bioquim, Lab Radioisotopes, RA-1113 Buenos Aires, DF, Argentina
关键词
coumarins; o-hydroxybenzaldehydes; Wittig reaction; natural products; structural revision; 6H-[1,3]dioxolo[4,5-g]chromen-6-ones;
D O I
10.1016/j.tet.2004.12.061
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of three highly oxygenated naturally occurring coumarins, 8-methoxy-6,7-methylenedioxycoumarin, 5-methoxy-6,7-methylenedioxycoumarin and 5,8-dimethoxy-6,7-methylenedioxycoumarin is described for the first time, together with a new method for the preparation of ayapin (6,7-methylenedioxycoumarin). Comparison of the spectroscopic data of the synthetic tetraoxygenated coumarin 5,8-dimethoxy-6,7-methylenedioxycoumarin with literature reports resulted in the structural revision of several natural coumarins. Two coumarins, both identified as 5,8-dimethoxy-6,7-methylenedioxycoumarin must have other structures, while the structure of another coumarin, described as the isomeric 7,8-dimethoxy-5,6-methylenedioxycoumarin has to be revised to 5,8-dimethoxy-6,7-methylenedioxy-coumarin. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2505 / 2511
页数:7
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