Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: borrowing hydrogen, returning carbon.

Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: borrowing hydrogen, returning carbon.
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DOI:
10.1002/anie.201403873
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发表时间:
2014-08-25
影响因子:
16.6
通讯作者:
Krische, Michael J.
Krische, Michael J.
中科院分区:
化学1区
文献类型:
--
作者:
Ketcham, John M.;Shin, Inji;Montgomery, T. Patrick;Krische, Michael J.

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醇和不饱和反应物用于氧化还原触发生成亲核-亲电对代表了羰基加成化学的一种广泛的新方法。离散氧化还原操作通常需要生成羰基亲电试剂和预金属化的碳中心亲核试剂,因此避免了。基于这一概念,一种广泛的、新的、由铱或钌配合物催化的对映选择性C - γ - C偶联反应被开发出来,本文对其进行了总结。
The use of alcohols and unsaturated reactants for the redox‐triggered generation of nucleophile–electrophile pairs represents a broad, new approach to carbonyl addition chemistry. Discrete redox manipulations that are often required for the generation of carbonyl electrophiles and premetalated carbon‐centered nucleophiles are thus avoided. Based on this concept, a broad, new family of enantioselective CC coupling reactions that are catalyzed by iridium or ruthenium complexes have been developed, which are summarized in this Minireview.
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