Synthesis of Non-Classical Arylated C-Saccharides through Nickel/Photoredox Dual Catalysis

被引:148
|
作者
Dumoulin, Audrey [1 ]
Matsui, Jennifer K. [1 ]
Gutierrez-Bonet, Alvaro [1 ]
Molander, Gary A. [1 ]
机构
[1] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA
关键词
1,4-dihydropyridines; glycosylation; homogeneous catalysis; nickel; photoredox chemistry; CROSS-COUPLING REACTIONS; GLYCOSIDES; ALKYLATION; RADICALS; 4-ALKYL-1,4-DIHYDROPYRIDINES; CONFORMATION; TECHNOLOGY; MECHANISM; REAGENTS;
D O I
10.1002/anie.201802282
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of synthetic tools to introduce saccharide derivatives into functionally complex molecules is of great interest, particularly in the field of drug discovery. Herein, we report a new route toward highly functionalized, arylated saccharides, which involves nickel-catalyzed cross-coupling of photoredox-generated saccharyl radicals with a range of aryl- and heteroaryl bromides, triggered by an organic photocatalyst. In contrast to existing methods, the mild reaction conditions achieve arylation of saccharide motifs while leaving the anomeric carbon available, thus providing access to a class of arylated glycosides that has been underexplored until now. To demonstrate the potential of this strategy in late-stage functionalization, a variety of structurally complex molecules incorporating saccharide moieties were synthesized.
引用
收藏
页码:6614 / 6618
页数:5
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