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三甲基吡唑辅助的铑(III)催化的β 或 γ C(sp)-H 单芳基化反应。

Rhodium(III)-Catalyzed Selective Monoarylation of β or γ C(sp)-H Bonds Assisted by a Trimethylpyrazole Group.

机构信息

Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University , Suzhou 215123, China.

出版信息

Org Lett. 2017 Jan 20;19(2):356-359. doi: 10.1021/acs.orglett.6b03522. Epub 2016 Dec 30.

Abstract

The selective arylation of unactivated β or challenging γ primary and secondary β-C(sp)-H bonds has been developed with a Cp*Rh(III) catalyst assisted by a trimethylpyrazole group. A rarely reported six-membered rhodacycle has been identified in rhodium-catalyzed C(sp)-H activation reactions. Preliminary mechanistic studies have revealed that a concerted metalation-deprotonation pathway might be involved in the C-H activation step.

摘要

具有三甲基吡唑基辅助的 Cp*Rh(III) 催化剂实现了未活化的β位或具有挑战性的γ位伯、仲β-C(sp)-H 键的选择性芳基化。在铑催化的 C(sp)-H 活化反应中,发现了一种罕见的六元铼环。初步的机理研究表明,C-H 活化步骤可能涉及协同的金属化-去质子化途径。

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