Recent advances in direct C-H arylation: Methodology, selectivity and mechanism in oxazole series.

Recent advances in direct C-H arylation: Methodology, selectivity and mechanism in oxazole series.
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DOI:
10.3762/bjoc.7.187
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发表时间:
2011
影响因子:
2.7
通讯作者:
Hoarau C
Hoarau C
中科院分区:
化学4区
文献类型:
--
作者:
Verrier C;Lassalas P;Théveau L;Quéguiner G;Trécourt F;Marsais F;Hoarau C

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(杂)芳烃的催化直接(杂)芳基化是传统Kumada、Stille、Negishi和Suzuki-Miyaura交叉偶联反应的有吸引力的替代方案,特别是因为它避免了(杂)芳基金属的预先制备和分离。本文综述了该方法在恶唑类化合物中的研究进展。介绍了方法学、选择性、机理和未来发展方向。
Catalytic direct (hetero)arylation of (hetero)arenes is an attractive alternative to traditional Kumada, Stille, Negishi and Suzuki–Miyaura cross-coupling reactions, notably as it avoids the prior preparation and isolation of (hetero)arylmetals. Developments of this methodology in the oxazole series are reviewed in this article. Methodologies, selectivity, mechanism and future aspects are presented.
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