期刊
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 10, 期 -, 页码 2981-2988出版社
BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.10.316
关键词
iminium salt; organometallic; oxidative functionalisation; photoredox catalysis; tetrahydroisoquinoline
资金
- GlaxoSmithKline
- University of Strathclyde
Nucleophilic trapping of iminium salts generated via oxidative functionalisation of tertiary amines is well established with stabilised carbon nucleophiles. The few reports of organometallic additions have limited scope of substrate and organometallic nucleophile. We report a novel, one-pot methodology that functionalises N-substituted tetrahydroisoquinolines by visible lightassisted photooxidation, followed by trapping of the resultant iminium ions with organometallic nucleophiles. This affords 1,2-disubstituted tetrahydroisoquinolines in moderate to excellent yields.
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