The Barbier−Grignard-Type Carbonyl Alkylation Using Unactivated Alkyl Halides in Water | Journal of the American Chemical Society
![Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja054706a/asset/images/medium/ja054706ah00003.gif)
Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society
![Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja054706a/asset/images/medium/ja054706ah00001.gif)
Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society
![Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja054706a/asset/images/medium/ja054706ah00002.gif)
Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society
![Zinc-mediated α-regioselective Barbier-type cinnamylation reactions of aldehydes, ketones and esters - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB00723J Zinc-mediated α-regioselective Barbier-type cinnamylation reactions of aldehydes, ketones and esters - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB00723J](https://pubs.rsc.org/image/article/2017/OB/c7ob00723j/c7ob00723j-s3_hi-res.gif)
Zinc-mediated α-regioselective Barbier-type cinnamylation reactions of aldehydes, ketones and esters - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB00723J
![Molecules | Free Full-Text | Zn Mediated Regioselective Barbier Reaction of Propargylic Bromides in THF/aq. NH4Cl Solution Molecules | Free Full-Text | Zn Mediated Regioselective Barbier Reaction of Propargylic Bromides in THF/aq. NH4Cl Solution](https://pub.mdpi-res.com/molecules/molecules-06-00964/article_deploy/html/images/molecules-06-00964-g001.png?1537430533)
Molecules | Free Full-Text | Zn Mediated Regioselective Barbier Reaction of Propargylic Bromides in THF/aq. NH4Cl Solution
![Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja054706a/asset/images/medium/ja054706ah00004.gif)
Nonradical Zinc−Barbier Reaction for Diastereoselective Synthesis of Vicinal Amino Alcohols | Journal of the American Chemical Society
![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
![A Mechanochemical Zinc-Mediated Barbier-Type Allylation Reaction under Ball-Milling Conditions | The Journal of Organic Chemistry A Mechanochemical Zinc-Mediated Barbier-Type Allylation Reaction under Ball-Milling Conditions | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.9b02876/asset/images/large/jo9b02876_0005.jpeg)
A Mechanochemical Zinc-Mediated Barbier-Type Allylation Reaction under Ball-Milling Conditions | The Journal of Organic Chemistry
![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/full/springer-static/image/art%3A10.1038%2Fncomms5254/MediaObjects/41467_2014_Article_BFncomms5254_Fig1_HTML.jpg)
The Barbier–Grignard-type arylation of aldehydes using unactivated aryl iodides in water | Nature Communications
![Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones - Chemical Science (RSC Publishing) DOI:10.1039/C8SC02038H Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones - Chemical Science (RSC Publishing) DOI:10.1039/C8SC02038H](https://pubs.rsc.org/image/article/2018/SC/c8sc02038h/c8sc02038h-s1_hi-res.gif)