Pd-Catalyzed Cyanoselenylation of Internal Alkynes: Access to Tetrasubstituted Selenoenol Ethers

被引:30
作者
Buerger, Marcel [1 ]
Roettger, Sebastian H. [1 ]
Loch, Maximilian N. [1 ]
Jones, Peter G. [2 ]
Werz, Daniel B. [1 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Organ Chem, D-38106 Braunschweig, Germany
[2] Tech Univ Carolo Wilhelmina Braunschweig, Inst Anorgan & Analyt Chem, D-38106 Braunschweig, Germany
关键词
CHALCOGEN-CHALCOGEN INTERACTIONS; HIGHLY REGIOSELECTIVE CYANOTHIOLATION; ANTI-CARBOPALLADATION; CASCADE REACTIONS; HELICAL ALKENES; DOMINO APPROACH; BONDS; THIOCYANATES; SEQUENCE; ISOCHROMANS;
D O I
10.1021/acs.orglett.0c01582
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The intra- and intermolecular synthesis of selenium-substituted acyclic and heterocyclic acrylonitrile derivatives is presented. The 1,2-difunctionalization of several internal alkynes substituted not only by aliphatic and aromatic residues but also by heteroelements is realized by the Pd-catalyzed activation of aromatic and aliphatic selenocyanates. A high functional group tolerance allows straightforward access to a broad scope of tetrasubstituted olefins. X-ray studies of some products reveal noncovalent chalcogen-chalcogen interactions between oxygen and selenium.
引用
收藏
页码:5025 / 5029
页数:5
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