New ligand platforms for developing the chemistry of the TiN–NR2 functional group and the insertion of alkynes into the N–N bond of a TiN–NPh2 ligand

Literature Information

Publication Date 2007-09-21
DOI 10.1039/B711941K
Impact Factor 6.222
Authors

Jonathan D. Selby, Catherine D. Manley, Marta Feliz, Andrew D. Schwarz, Eric Clot, Philip Mountford


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Abstract

Two broadly applicable strategies for extending the available ligand platforms of the virtually unexplored terminal TiN–NR2 functional group are described, along with the highly selective room temperature insertion of alkynes into the N–N bond of Ti{MeN(CH2CH2NSiMe3)2}(NNPh2)(py) and the catalytic cis-diamination of PhCCMe by diphenylhydrazine.

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Chemical Communications

Chemical Communications
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ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry

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