AN EXPEDIENT ROUTE TO INDOLE-3-ACETIC-ACID DERIVATIVES

被引:0
作者
SAMIZU, K [1 ]
OGASAWARA, K [1 ]
机构
[1] TOHOKU UNIV,INST PHARMACEUT,SENDAI 98077,JAPAN
关键词
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An expedient synthesis of indole-3-acetic acid derivatives has been developed by employing the Heck reaction between 2-iodoaniline derivatives and 2,5-dihydro-dimethoxyfuran as the key step.
引用
收藏
页码:499 / 500
页数:2
相关论文
共 5 条
[1]   AMIDOMERCURATION-CYCLIZATION OF N-TERT-BUTOXYCARBONYL-2-ALLYLANILINE DERIVATIVES [J].
BERGER, J ;
KERLY, DL .
HETEROCYCLES, 1993, 36 (09) :2051-2058
[2]   THE SYNTHESIS OF CERTAIN SUBSTITUTED INDOLEACETIC ACIDS [J].
FINDLAY, SP ;
DOUGHERTY, G .
JOURNAL OF ORGANIC CHEMISTRY, 1948, 13 (04) :560-569
[3]  
HEC RF, 1977, TETRAHEDRON LETT, P1037
[4]   RAPID SYNTHESES OF SOME INDOLE ALKALOIDS OF THE CALABAR BEAN [J].
HORNE, S ;
TAYLOR, N ;
COLLINS, S ;
RODRIGO, R .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1991, (12) :3047-3051
[5]   CARBON-DIOXIDE - A REAGENT FOR THE SIMULTANEOUS PROTECTION OF NUCLEOPHILIC CENTERS AND THE ACTIVATION OF ALTERNATIVE LOCATIONS TO ELECTROPHILIC ATTACK - .3. A NEW SYNTHETIC METHOD FOR THE ORTHO-SUBSTITUTION OF N-MONOALKYLANILINES [J].
KATRITZKY, AR ;
FAN, WQ ;
AKUTAGAWA, K .
TETRAHEDRON, 1986, 42 (14) :4027-4034