Catalytic and structural studies of hoveyda-grubbs type pre-catalysts bearing modified ether ligands

Stefano Guidone; Enguerr Blondiaux; Cezary Samojłowicz; Łukasz Gułajski; Mariusz Ke Dziorek; Maura Malińska; Aleksandra Pazio; Krzysztof Woźniak; Karol Grela; Angelino Doppiu; Catherine S.J. Cazin

doi:10.1002/adsc.201200385

Catalytic and structural studies of hoveyda-grubbs type pre-catalysts bearing modified ether ligands

Stefano Guidone, Enguerr Blondiaux, Cezary Samojłowicz, Łukasz Gułajski, Mariusz Ke Dziorek, Maura Malińska, Aleksandra Pazio, Krzysztof Woźniak, Karol Grela, Angelino Doppiu, Catherine S.J. Cazin

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

18 Scopus citations

Abstract

Catalytic and crystallographic studies of Hoveyda-Grubbs type pre-catalysts M51TM and M52TM were performed. These two new instruments in the olefin metathesis catalyst toolbox were shown to be active at ambient temperature and at low loading, leading to clean formation of ring-closing, ringclosing enyne and cross metathesis products.

Original language	English
Pages (from-to)	2734-2742
Number of pages	9
Journal	Advanced Synthesis and Catalysis
Volume	354
Issue number	14-15
DOIs	https://doi.org/10.1002/adsc.201200385
State	Published - 8 Oct 2012
Externally published	Yes

Keywords

N-heterocyclic carbenes
Olefin metathesis
Ring-closing metathesis
Ruthenium

ASJC Scopus subject areas

Catalysis
Organic Chemistry

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10.1002/adsc.201200385

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title = "Catalytic and structural studies of hoveyda-grubbs type pre-catalysts bearing modified ether ligands",

abstract = "Catalytic and crystallographic studies of Hoveyda-Grubbs type pre-catalysts M51TM and M52TM were performed. These two new instruments in the olefin metathesis catalyst toolbox were shown to be active at ambient temperature and at low loading, leading to clean formation of ring-closing, ringclosing enyne and cross metathesis products.",

keywords = "N-heterocyclic carbenes, Olefin metathesis, Ring-closing metathesis, Ruthenium",

author = "Stefano Guidone and Enguerr Blondiaux and Cezary Samoj{\l}owicz and {\L}ukasz Gu{\l}ajski and Dziorek, {Mariusz Ke} and Maura Mali{\'n}ska and Aleksandra Pazio and Krzysztof Wo{\'z}niak and Karol Grela and Angelino Doppiu and Cazin, {Catherine S.J.}",

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doi = "10.1002/adsc.201200385",

language = "English",

volume = "354",

pages = "2734--2742",

journal = "Advanced Synthesis and Catalysis",

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TY - JOUR

T1 - Catalytic and structural studies of hoveyda-grubbs type pre-catalysts bearing modified ether ligands

AU - Guidone, Stefano

AU - Blondiaux, Enguerr

AU - Samojłowicz, Cezary

AU - Gułajski, Łukasz

AU - Dziorek, Mariusz Ke

AU - Malińska, Maura

AU - Pazio, Aleksandra

AU - Woźniak, Krzysztof

AU - Grela, Karol

AU - Doppiu, Angelino

AU - Cazin, Catherine S.J.

PY - 2012/10/8

Y1 - 2012/10/8

N2 - Catalytic and crystallographic studies of Hoveyda-Grubbs type pre-catalysts M51TM and M52TM were performed. These two new instruments in the olefin metathesis catalyst toolbox were shown to be active at ambient temperature and at low loading, leading to clean formation of ring-closing, ringclosing enyne and cross metathesis products.

AB - Catalytic and crystallographic studies of Hoveyda-Grubbs type pre-catalysts M51TM and M52TM were performed. These two new instruments in the olefin metathesis catalyst toolbox were shown to be active at ambient temperature and at low loading, leading to clean formation of ring-closing, ringclosing enyne and cross metathesis products.

KW - N-heterocyclic carbenes

KW - Olefin metathesis

KW - Ring-closing metathesis

KW - Ruthenium

UR - http://www.scopus.com/inward/record.url?scp=84869026780&partnerID=8YFLogxK

U2 - 10.1002/adsc.201200385

DO - 10.1002/adsc.201200385

M3 - Article

AN - SCOPUS:84869026780

SN - 1615-4150

VL - 354

SP - 2734

EP - 2742

JO - Advanced Synthesis and Catalysis

JF - Advanced Synthesis and Catalysis

IS - 14-15

ER -

Catalytic and structural studies of hoveyda-grubbs type pre-catalysts bearing modified ether ligands

Abstract

Keywords

ASJC Scopus subject areas

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