![Scheme 55. Reagents: i, LiHMDS, THF, –78ºC; ii, oiodobenzaldehyde ;... | Download Scientific Diagram Scheme 55. Reagents: i, LiHMDS, THF, –78ºC; ii, oiodobenzaldehyde ;... | Download Scientific Diagram](https://www.researchgate.net/publication/229014398/figure/fig3/AS:393821901869056@1470905866096/Scheme-55-Reagents-i-LiHMDS-THF-78C-ii-oiodobenzaldehyde-iii-Me-3-SiCl-iv.png)
Scheme 55. Reagents: i, LiHMDS, THF, –78ºC; ii, oiodobenzaldehyde ;... | Download Scientific Diagram
Cyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones | Journal of the American Chemical Society
![Lithium Hexamethyldisilazide-Mediated Enolization of Highly Substituted Aryl Ketones: Structural and Mechanistic Basis of the E/Z Selectivities. - Abstract - Europe PMC Lithium Hexamethyldisilazide-Mediated Enolization of Highly Substituted Aryl Ketones: Structural and Mechanistic Basis of the E/Z Selectivities. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6122874/bin/nihms-981932-f0025.jpg)
Lithium Hexamethyldisilazide-Mediated Enolization of Highly Substituted Aryl Ketones: Structural and Mechanistic Basis of the E/Z Selectivities. - Abstract - Europe PMC
![LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1566736720302703-ga1.jpg)
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect
![LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1566736720302703-sc2.jpg)
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect
![Scheme5.Reagents and conditions: a) 13,LiHMDS, THF, À78 8C; then add... | Download Scientific Diagram Scheme5.Reagents and conditions: a) 13,LiHMDS, THF, À78 8C; then add... | Download Scientific Diagram](https://www.researchgate.net/publication/318871359/figure/fig1/AS:567054076203008@1512207635181/Scheme5Reagents-and-conditions-a-13-LiHMDS-THF-A78-8C-then-add-aldehyde-b-TBSCl.png)
Scheme5.Reagents and conditions: a) 13,LiHMDS, THF, À78 8C; then add... | Download Scientific Diagram
![Cyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones | Journal of the American Chemical Society Cyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c13231/asset/images/large/ja0c13231_0004.jpeg)
Cyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones | Journal of the American Chemical Society
![Cyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones | Journal of the American Chemical Society Cyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c13231/asset/images/large/ja0c13231_0005.jpeg)
Cyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones | Journal of the American Chemical Society
![LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1566736720302703-sc5.jpg)
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect
![Lithium hexamethyldisilazide-mediated enolizations: influence of triethylamine on E/Z selectivities and enolate reactivities. - Abstract - Europe PMC Lithium hexamethyldisilazide-mediated enolizations: influence of triethylamine on E/Z selectivities and enolate reactivities. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3021125/bin/nihms56225f5.jpg)
Lithium hexamethyldisilazide-mediated enolizations: influence of triethylamine on E/Z selectivities and enolate reactivities. - Abstract - Europe PMC
![Lithium hexamethyldisilazide initiated superfast ring opening polymerization of alpha-amino acid N-carboxyanhydrides | Nature Communications Lithium hexamethyldisilazide initiated superfast ring opening polymerization of alpha-amino acid N-carboxyanhydrides | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-018-07711-y/MediaObjects/41467_2018_7711_Fig1_HTML.png)