Literature DB >> 25802009

Z-selective cross metathesis with ruthenium catalysts: synthetic applications and mechanistic implications.

Myles B Herbert1, Robert H Grubbs.   

Abstract

Olefin cross metathesis is a particularly powerful transformation that has been exploited extensively for the formation of complex products. Until recently, however, constructing Z-olefins using this methodology was not possible. With the discovery and development of three families of ruthenium-based Z-selective catalysts, the formation of Z-olefins using metathesis is now not only possible but becoming increasingly prevalent in the literature. In particular, ruthenium complexes containing cyclometalated NHC architectures developed in our group have been shown to catalyze various cross metathesis reactions with high activity and, in most cases, near perfect selectivity for the Z-isomer. The types of cross metathesis reactions investigated thus far are presented here and explored in depth.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Z-alkenes; cross metathesis; natural products; olefin metathesis

Year:  2015        PMID: 25802009     DOI: 10.1002/anie.201411588

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  13 in total

1.  Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction.

Authors:  Cheoljae Kim; Hoyong Chung
Journal:  J Vis Exp       Date:  2018-08-23       Impact factor: 1.355

2.  Molybdenum chloride catalysts for Z-selective olefin metathesis reactions.

Authors:  Ming Joo Koh; Thach T Nguyen; Jonathan K Lam; Sebastian Torker; Jakub Hyvl; Richard R Schrock; Amir H Hoveyda
Journal:  Nature       Date:  2017-01-23       Impact factor: 49.962

3.  Synthesis of 9-Dechlorochrysophaentin A Enables Studies Revealing Bacterial Cell Wall Biosynthesis Inhibition Phenotype in B. subtilis.

Authors:  Christopher R Fullenkamp; Yen-Pang Hsu; Ellen M Quardokus; Gengxiang Zhao; Carole A Bewley; Michael VanNieuwenhze; Gary A Sulikowski
Journal:  J Am Chem Soc       Date:  2020-09-08       Impact factor: 15.419

4.  Tandem Olefin Metathesis/Oxidative Cyclization: Synthesis of Tetrahydrofuran Diols from Simple Olefins.

Authors:  Peter K Dornan; Daniel Lee; Robert H Grubbs
Journal:  J Am Chem Soc       Date:  2016-05-11       Impact factor: 15.419

5.  Single-chain polybutadiene organometallic nanoparticles: an experimental and theoretical study.

Authors:  Inbal Berkovich; Sudheendran Mavila; Olga Iliashevsky; Sebastian Kozuch; N Gabriel Lemcoff
Journal:  Chem Sci       Date:  2016-01-07       Impact factor: 9.825

6.  Identification, synthesis and mass spectrometry of a macrolide from the African reed frog Hyperolius cinnamomeoventris.

Authors:  Markus Menke; Pardha Saradhi Peram; Iris Starnberger; Walter Hödl; Gregory Fm Jongsma; David C Blackburn; Mark-Oliver Rödel; Miguel Vences; Stefan Schulz
Journal:  Beilstein J Org Chem       Date:  2016-12-13       Impact factor: 2.883

7.  Amide-Directed Formation of Five-Coordinate Osmium Alkylidenes from Alkynes.

Authors:  Noelia Casanova; Miguel A Esteruelas; Moisés Gulías; Carmen Larramona; José L Mascareñas; Enrique Oñate
Journal:  Organometallics       Date:  2015-12-31       Impact factor: 3.876

8.  Cationic ruthenium alkylidene catalysts bearing phosphine ligands.

Authors:  Koji Endo; Robert H Grubbs
Journal:  Dalton Trans       Date:  2016-02-28       Impact factor: 4.390

9.  Cross metathesis of unsaturated epoxides for the synthesis of polyfunctional building blocks.

Authors:  Meriem K Abderrezak; Kristýna Šichová; Nancy Dominguez-Boblett; Antoine Dupé; Zahia Kabouche; Christian Bruneau; Cédric Fischmeister
Journal:  Beilstein J Org Chem       Date:  2015-10-08       Impact factor: 2.883

10.  Synthesis of the C(1)-C(13) Fragment of Leiodermatolide via Hydrogen-Mediated C-C Bond Formation.

Authors:  James Roane; Julian Wippich; Stephen D Ramgren; Michael J Krische
Journal:  Org Lett       Date:  2017-11-23       Impact factor: 6.005

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