Revised Mechanism for a Ruthenium-Catalyzed Coupling of Aldehyde and Terminal Alkyne-Reference-Cited by-同舟云学术

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Revised Mechanism for a Ruthenium-Catalyzed Coupling of Aldehyde and Terminal Alkyne

Published:2018-03-16 Issue:3 Volume:3 Page:3218-3227
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Tomberg Anna¹,Kundu Soumen¹,Zhou Feng¹,Li Chao-Jun¹^ORCID,Moitessier Nicolas¹^ORCID

Affiliation:

1. Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, Montréal, Quebec, Canada H3A 0B8

Funder

Canada Foundation for Innovation

Fonds de Recherche du Qu?bec - Nature et Technologies

Canada Research Chairs

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.7b01877

Reference76 articles.

1. New Synthetic Methodologies for Carbon−Carbon Double Bond Formation

2. ‘Phospha-variations’ on the themes of Staudinger and Wittig: phosphorus analogs of Wittig reagents

3. An expedient approach to E,Z-dienes using the Julia olefination

4. Highly (E)-Selective Wadsworth−Emmons Reactions Promoted by Methylmagnesium Bromide

5. Stereoselective Synthesis of Polysubstituted Alkenes through a Phosphine-Mediated Three-Component System of Aldehydes, α-Halo Carbonyl Compounds, and Terminal Alkenes

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1. Ru-Catalyzed and Selenium-Directed Selective Formation of ortho- and Dialkenylated Selanes, Mixed Organoselenoethers, and Isoselenochromenes;Organic Letters;2024-02-22

2. Cationic Iridium‐Catalyzed Asymmetric Decarbonylative Aryl Addition of Aromatic Aldehydes to Bicyclic Alkenes;Chemistry – A European Journal;2022-01-28

3. Recent advancements on decarbonylation reactions assisted by Ru-complexes: Synthetic and mechanistic approach;Dalton Transactions;2022

4. Visible-light-induced transition metal and photosensitizer free decarbonylative addition of amino-arylaldehydes to ketones;Chemical Science;2022

5. Oxetanes and Oxetenes: Fused-Ring Derivatives;Comprehensive Heterocyclic Chemistry IV;2022

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