A NEW METHOD FOR GENERATION OF 4-ARYL AND 6-ARYL THIENO[2,3-C]FURANS, AND 3-ARYL FURO[3,4-B]PYRIDINE

被引:28
作者
KURODA, T [1 ]
TAKAHASHI, M [1 ]
OGIKU, T [1 ]
OHMIZU, H [1 ]
KONDO, K [1 ]
IWASAKI, T [1 ]
机构
[1] TANABE SEIYAKU CO LTD,DEPT SYNTHET CHEM,APPL BIOCHEM RES LAB,3-16-89 KASHIMA,YODOGAWA KU,OSAKA 532,JAPAN
关键词
D O I
10.1039/c39910001635
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
6-Aryl thieno[2,3-c]furans 2a-c, 4-(3,4-dimethoxyphenyl)thieno[2,3-c]furan 3a, and 3-(3,4-dimethoxyphenyl)furo[3,4-b]pyridine 4a, which were intercepted in situ by dimethyl acetylenedicarboxylate to give the corresponding Diels-Alder adducts in good yields, were generated under acidic conditions from 2-(alpha-acetoxybenzyl)thiophene-3-carbaldehydes 5a-c, 3-(alpha-acetoxy-3,4-dimethoxybenzyl)thiophene-2-carbaldehyde 10a and 2-(alpha-acetoxy-3,4-dimethoxybenzyl)pyridine-3-carbaldehyde 12a, respectively.
引用
收藏
页码:1635 / 1636
页数:2
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