Literature DB >> 28599101

Stereoretentive Olefin Metathesis: An Avenue to Kinetic Selectivity.

T Patrick Montgomery1, Tonia S Ahmed1, Robert H Grubbs1.   

Abstract

Olefin metathesis is an incredibly valuable transformation that has gained widespread use in both academic and industrial settings. Lately, stereoretentive olefin metathesis has garnered much attention as a method for the selective generation of both E- and Z-olefins. Early studies employing ill-defined catalysts showed evidence for retention of the stereochemistry of the starting olefins at low conversion. However, thermodynamic ratios E/Z were reached as the reaction proceeded to equilibrium. Recent studies in olefin metathesis have focused on the synthesis of catalysts that can overcome the inherent thermodynamic preference of an olefin, providing synthetically useful quantities of a kinetically favored olefin isomer. These reports have led to the development of stereoretentive catalysts that not only generate Z-olefins selectively, but also kinetically produce E-olefins, a previously unmet challenge in olefin metathesis. Advancements in stereoretentive olefin metathesis using tungsten, ruthenium, and molybdenum catalysts are presented.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  molybdenum; olefin metathesis; ruthenium; stereoretention; tungsten

Mesh:

Substances:

Year:  2017        PMID: 28599101     DOI: 10.1002/anie.201704686

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


  9 in total

1.  Traceless Protection for More Broadly Applicable Olefin Metathesis.

Authors:  Yucheng Mu; Thach T Nguyen; Farid W van der Mei; Richard R Schrock; Amir H Hoveyda
Journal:  Angew Chem Int Ed Engl       Date:  2019-03-13       Impact factor: 15.336

2.  Novel Cyclic Biphalin Analogues by Ruthenium-Catalyzed Ring Closing Metathesis: in Vivo and in Vitro Biological Profile.

Authors:  Azzurra Stefanucci; Wei Lei; Stefano Pieretti; Marilisa Pia Dimmito; Grazia Luisi; Ettore Novellino; Michał Nowakowski; Wiktor Koźmiński; Sako Mirzaie; Gokhan Zengin; John M Streicher; Adriano Mollica
Journal:  ACS Med Chem Lett       Date:  2019-03-08       Impact factor: 4.345

3.  Dipicolinate Complexes of Oxovanadium(IV) and Dioxovanadium(V) with 2-Phenylpyridine and 4,4'-Dimethoxy-2,2'-bipyridyl as New Precatalysts for Olefin Oligomerization.

Authors:  Joanna Drzeżdżon; Marta Pawlak; Barbara Gawdzik; Aleksandra Wypych; Karol Kramkowski; Paweł Kowalczyk; Dagmara Jacewicz
Journal:  Materials (Basel)       Date:  2022-02-13       Impact factor: 3.623

4.  Using stereoretention for the synthesis of E-macrocycles with ruthenium-based olefin metathesis catalysts.

Authors:  Tonia S Ahmed; T Patrick Montgomery; Robert H Grubbs
Journal:  Chem Sci       Date:  2018-03-14       Impact factor: 9.825

5.  Highly active ruthenium metathesis catalysts enabling ring-opening metathesis polymerization of cyclopentadiene at low temperatures.

Authors:  Kitaek Song; Kunsoon Kim; Daeun Hong; Jungwon Kim; Chae Eun Heo; Hugh I Kim; Soon Hyeok Hong
Journal:  Nat Commun       Date:  2019-08-27       Impact factor: 14.919

6.  A Simple Nickel Catalyst Enabling an E-Selective Alkyne Semihydrogenation.

Authors:  Niklas O Thiel; Benyapa Kaewmee; Trung Tran Ngoc; Johannes F Teichert
Journal:  Chemistry       Date:  2020-01-21       Impact factor: 5.236

Review 7.  Combining enyne metathesis with long-established organic transformations: a powerful strategy for the sustainable synthesis of bioactive molecules.

Authors:  Valerian Dragutan; Ileana Dragutan; Albert Demonceau; Lionel Delaude
Journal:  Beilstein J Org Chem       Date:  2020-04-16       Impact factor: 2.883

8.  The Ascent of Alkyne Metathesis to Strategy-Level Status.

Authors:  Alois Fürstner
Journal:  J Am Chem Soc       Date:  2021-09-14       Impact factor: 15.419

9.  Light-Activated Olefin Metathesis: Catalyst Development, Synthesis, and Applications.

Authors:  Or Eivgi; Ravindra S Phatake; Noy B Nechmad; N Gabriel Lemcoff
Journal:  Acc Chem Res       Date:  2020-09-29       Impact factor: 22.384

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.