C2-symmetric zirconium Bis(Amidate) complexes with enhanced reactivity in aminoalkene hydroamination

Alexander L. Reznichenko; Kai C. Hultzsch

doi:10.1021/om9008907

C2-symmetric zirconium Bis(Amidate) complexes with enhanced reactivity in aminoalkene hydroamination

Alexander L. Reznichenko
, Kai C. Hultzsch

Not published at VTT

Rutgers - The State University of New Jersey

Research output: Contribution to journal › Article › Scientific › peer-review

97 Citations (Scopus)

Abstract

Binaphthalenedicarboxamide zirconium complexes exhibit significantly enhanced catalytic activity in aminoalkene hydroamination reactions with respect to substrate scope (substrates without gem-dialkyl activation; cyclization of aminoheptenes), catalyst loading (as low as 0.5 mol %) and reaction temperatures (as low as 70 °C) compared to previous group 4 metal-based hydroamination catalyst systems.

Original language	English
Pages (from-to)	24-27
Number of pages	4
Journal	Organometallics
Volume	29
Issue number	1
DOIs	https://doi.org/10.1021/om9008907
Publication status	Published - 11 Jan 2010
MoE publication type	A1 Journal article-refereed

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10.1021/om9008907

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title = "C2-symmetric zirconium Bis(Amidate) complexes with enhanced reactivity in aminoalkene hydroamination",

abstract = "Binaphthalenedicarboxamide zirconium complexes exhibit significantly enhanced catalytic activity in aminoalkene hydroamination reactions with respect to substrate scope (substrates without gem-dialkyl activation; cyclization of aminoheptenes), catalyst loading (as low as 0.5 mol \%) and reaction temperatures (as low as 70 °C) compared to previous group 4 metal-based hydroamination catalyst systems.",

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AU - Reznichenko, Alexander L.

AU - Hultzsch, Kai C.

PY - 2010/1/11

Y1 - 2010/1/11

N2 - Binaphthalenedicarboxamide zirconium complexes exhibit significantly enhanced catalytic activity in aminoalkene hydroamination reactions with respect to substrate scope (substrates without gem-dialkyl activation; cyclization of aminoheptenes), catalyst loading (as low as 0.5 mol %) and reaction temperatures (as low as 70 °C) compared to previous group 4 metal-based hydroamination catalyst systems.

AB - Binaphthalenedicarboxamide zirconium complexes exhibit significantly enhanced catalytic activity in aminoalkene hydroamination reactions with respect to substrate scope (substrates without gem-dialkyl activation; cyclization of aminoheptenes), catalyst loading (as low as 0.5 mol %) and reaction temperatures (as low as 70 °C) compared to previous group 4 metal-based hydroamination catalyst systems.

UR - https://www.scopus.com/pages/publications/73649113440

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DO - 10.1021/om9008907

M3 - Article

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JO - Organometallics

JF - Organometallics

IS - 1

ER -

C2-symmetric zirconium Bis(Amidate) complexes with enhanced reactivity in aminoalkene hydroamination

Abstract

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