![Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C](https://pubs.rsc.org/image/article/2017/RA/c6ra28631c/c6ra28631c-s1_hi-res.gif)
Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C
![Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C](https://pubs.rsc.org/image/article/2017/RA/c6ra28631c/c6ra28631c-u22_hi-res.gif)
Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C
Lithium Hexamethyldisilazide-Mediated Enolization of Acylated Oxazolidinones: Solvent, Cosolvent, and Isotope Effects on Competi
![Equilibrium Constants and Alkylation Kinetics of Two Lithium Enolates/LiHMDS Mixed Aggregates in THF | Organic Letters Equilibrium Constants and Alkylation Kinetics of Two Lithium Enolates/LiHMDS Mixed Aggregates in THF | Organic Letters](https://pubs.acs.org/cms/10.1021/ol017175d/asset/images/large/ol017175dn00001.jpeg)
Equilibrium Constants and Alkylation Kinetics of Two Lithium Enolates/LiHMDS Mixed Aggregates in THF | Organic Letters
![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
![Reaction of Ketones with Lithium Hexamethyldisilazide: Competitive Enolizations and 1,2-Additions | Journal of the American Chemical Society Reaction of Ketones with Lithium Hexamethyldisilazide: Competitive Enolizations and 1,2-Additions | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja030582v/asset/images/large/ja030582vn00001.jpeg)
Reaction of Ketones with Lithium Hexamethyldisilazide: Competitive Enolizations and 1,2-Additions | Journal of the American Chemical Society
![Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C](https://pubs.rsc.org/image/article/2017/RA/c6ra28631c/c6ra28631c-s2_hi-res.gif)
Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C
![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
![Scheme 34 Reagents and condition—a (i) LiHMDS, THF, −78 °C; (ii) R 2 CH... | Download Scientific Diagram Scheme 34 Reagents and condition—a (i) LiHMDS, THF, −78 °C; (ii) R 2 CH... | Download Scientific Diagram](https://www.researchgate.net/publication/317212042/figure/fig9/AS:499396430307336@1496076795796/Scheme-34-Reagents-and-condition-a-i-LiHMDS-THF-78-C-ii-R-2-CH-NPh-78-C-to.png)
Scheme 34 Reagents and condition—a (i) LiHMDS, THF, −78 °C; (ii) R 2 CH... | Download Scientific Diagram
![Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C](https://pubs.rsc.org/image/article/2017/RA/c6ra28631c/c6ra28631c-s4_hi-res.gif)
Efficient synthesis of novel N -substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation rea ... - RSC Advances (RSC Publishing) DOI:10.1039/C6RA28631C
![Scheme 15. Synthesis of AM281 (74). Reagents and conditions: (a) (i)... | Download Scientific Diagram Scheme 15. Synthesis of AM281 (74). Reagents and conditions: (a) (i)... | Download Scientific Diagram](https://www.researchgate.net/profile/Hiroki-Ishiguro-2/publication/7272098/figure/fig5/AS:431224108916740@1479823247328/Scheme-15-Synthesis-of-AM281-74-Reagents-and-conditions-a-i-LiHMDS-THF-ii-EtO_Q640.jpg)
Scheme 15. Synthesis of AM281 (74). Reagents and conditions: (a) (i)... | Download Scientific Diagram
![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
![Highly selective transition-metal-free transamidation of amides and amidation of esters at room temperature | Nature Communications Highly selective transition-metal-free transamidation of amides and amidation of esters at room temperature | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-018-06623-1/MediaObjects/41467_2018_6623_Fig6_HTML.png)