Titanium-Catalyzed Hydroamination and Multicomponent Coupling with a Simple Silica-Supported Catalyst

被引:19
作者
Aldrich, Kelly E. [1 ]
Odom, Aaron L. [1 ]
机构
[1] Michigan State Univ, Dept Chem, 578 South Shaw Lane, E Lansing, MI 48823 USA
基金
美国国家科学基金会;
关键词
INTERMOLECULAR HYDROAMINATION; COMPLEXES; ZIRCONIUM; ALKYNES; CHEMISTRY; MECHANISM; INSIGHTS;
D O I
10.1021/acs.organomet.8b00313
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Hydroamination and multicomponent coupling reactions catalyzed by homogeneous Ti(IV) complexes can produce valuable imines, amines, and other nitrogen-containing organic building blocks. Typically catalysts for this transformation are very sensitive to ancillary ligand design and often suffer from catalyst deactivation, necessitating use in a single reaction. Here, we have attempted to address these issues by moving toward a solid-supported Ti catalyst active for these reaction types. We present initial results to synthesize and probe the catalytic reactivity of silica-supported titanium amide precatalysts. With minimal treatment of commercially available fumed silica, Ti(NMe2)(2)/SiO2200 can be isolated upon addition of Ti(NMe2)(4). This species gives high yields and high regioselectivity for hydroamination of a variety of alkynes with anilines. The solid-supported species is also an active catalyst for the formation of tautomers of unsymmetrical 1,3-diimines via three-component coupling of bulky anilines, alkynes, and isonitriles. Reusability and possible catalyst deactivation pathways are also discussed.
引用
收藏
页码:4341 / 4349
页数:9
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