![Highly Selective Barbier‐Type Propargylations and Allenylations Catalyzed by Titanocene(III) - Muñoz‐Bascón - 2012 - Chemistry – A European Journal - Wiley Online Library Highly Selective Barbier‐Type Propargylations and Allenylations Catalyzed by Titanocene(III) - Muñoz‐Bascón - 2012 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/7b146e8b-ac89-4953-bd9d-0ab9411fa3f9/mcontent.jpg)
Highly Selective Barbier‐Type Propargylations and Allenylations Catalyzed by Titanocene(III) - Muñoz‐Bascón - 2012 - Chemistry – A European Journal - Wiley Online Library
![The Barbier‐Type Allylation/Lactamization Cascade Route to Isoindolinones and the Heck‐Type Annulation Route to Isoindolo[2,1‐a]quinolines - Reddy - 2016 - ChemistrySelect - Wiley Online Library The Barbier‐Type Allylation/Lactamization Cascade Route to Isoindolinones and the Heck‐Type Annulation Route to Isoindolo[2,1‐a]quinolines - Reddy - 2016 - ChemistrySelect - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/b06b178c-94ea-4876-bedf-f67485944662/slct201600411-toc-0001-m.jpg)
The Barbier‐Type Allylation/Lactamization Cascade Route to Isoindolinones and the Heck‐Type Annulation Route to Isoindolo[2,1‐a]quinolines - Reddy - 2016 - ChemistrySelect - Wiley Online Library
A Mechanochemical Zinc-Mediated Barbier-Type Allylation Reaction under Ball-Milling Conditions - UCL Discovery
![Mild and efficient barbier allylation reaction mediated by magnesium powder under solvent-free conditions - ScienceDirect Mild and efficient barbier allylation reaction mediated by magnesium powder under solvent-free conditions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402010018600-fx1.jpg)
Mild and efficient barbier allylation reaction mediated by magnesium powder under solvent-free conditions - ScienceDirect
![Scheme 2. Different products obtained under Barbier reaction conditions... | Download Scientific Diagram Scheme 2. Different products obtained under Barbier reaction conditions... | Download Scientific Diagram](https://www.researchgate.net/publication/333524334/figure/fig2/AS:764804306317312@1559354964414/Scheme-2-Different-products-obtained-under-Barbier-reaction-conditions-in-ionic-liquids_Q640.jpg)
Scheme 2. Different products obtained under Barbier reaction conditions... | Download Scientific Diagram
![PDF] Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc02038h | Semantic Scholar PDF] Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc02038h | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/4e47c016d4cbb1df10c98e9abd9c1a88b9bc05b4/5-Figure1-1.png)
PDF] Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc02038h | Semantic Scholar
![The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fncomms5254/MediaObjects/41467_2014_Article_BFncomms5254_Fig5_HTML.jpg)
The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications
![The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fncomms5254/MediaObjects/41467_2014_Article_BFncomms5254_Fig3_HTML.jpg)
The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications
![Ultrasound promoted Barbier reactions and Csp3–Csp2 Stille coupling for the synthesis of diarylmethanes and substituted benzophenones - ScienceDirect Ultrasound promoted Barbier reactions and Csp3–Csp2 Stille coupling for the synthesis of diarylmethanes and substituted benzophenones - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S135041771200137X-fx1.jpg)
Ultrasound promoted Barbier reactions and Csp3–Csp2 Stille coupling for the synthesis of diarylmethanes and substituted benzophenones - ScienceDirect
![The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fncomms5254/MediaObjects/41467_2014_Article_BFncomms5254_Fig2_HTML.jpg)
The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications
![Hydride as a Leaving Group in the Reaction of Pinacolborane with Halides under Ambient Grignard and Barbier Conditions. One-Pot Synthesis of Alkyl, Aryl, Heteroaryl, Vinyl, and Allyl Pinacolboronic Esters | The Journal Hydride as a Leaving Group in the Reaction of Pinacolborane with Halides under Ambient Grignard and Barbier Conditions. One-Pot Synthesis of Alkyl, Aryl, Heteroaryl, Vinyl, and Allyl Pinacolboronic Esters | The Journal](https://pubs.acs.org/cms/10.1021/jo201093u/asset/images/medium/jo-2011-01093u_0009.gif)