Palladium-Catalyzed Synthesis of Carbo- and Heterocycles through Norbornene-Mediated ortho C-H Functionalization

被引:72
|
作者
Ferraccioli, Raffaella [1 ]
机构
[1] CNR, ISTM, I-20133 Milan, Italy
来源
SYNTHESIS-STUTTGART | 2013年 / 45卷 / 05期
关键词
palladacycle; norbornene; C-H arylation; C-H alkylation; polycycles; ALKYLATION-ALKENYLATION REACTIONS; TETRASUBSTITUTED HELICAL ALKENES; SUBSTITUTED ARYL IODIDES; CROSS-COUPLING REACTIONS; NITROGEN-CONTAINING HETEROCYCLES; ONE-STEP SYNTHESIS; DIRECT ARYLATION; STEREOSELECTIVE-SYNTHESIS; EXPEDITIOUS SYNTHESIS; BOND FORMATION;
D O I
10.1055/s-0032-1318218
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Direct aromatic functionalization based on the use of a palladium catalyst and norbornene is a useful method to achieve straightforward synthesis of carbo- and heterocyclic compounds. New ring formation occurs through a cascade process triggered by ortho C-H alkylation (inter- and intramolecular) or arylation (homo- and heterocoupling) of aryl iodides. Up to four new carbon-carbon bonds are generated under palladium control in a single operation.
引用
收藏
页码:581 / 591
页数:11
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