噻吩
催化作用
选择性
化学
表面改性
组合化学
有机化学
药物化学
物理化学
作者
Kirika Ueda,Shuichi Yanagisawa,Junichiro Yamaguchi,Kenichiro Itami
标识
DOI:10.1002/anie.201005082
摘要
Open access: The normally less-reactive β position of thiophenes was previously inaccessible to direct functionalization. However, the β selectivity observed with the catalytic system PdCl2/P{OCH(CF3)2}3/Ag2CO3 in the arylation of thiophenes with iodoarenes (see scheme) is a remarkably general phenomenon applicable to unsubstituted, monosubstituted, and disubstituted thiophene derivatives, as well as thiophene-containing fused aromatic compounds.
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