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Lithium Bis(trimethylsilyl)amide (LiHMDS)
Lithium Bis(trimethylsilyl)amide (LiHMDS)

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

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

Lithium bis(trimethylsilyl)amide - Wikipedia
Lithium bis(trimethylsilyl)amide - Wikipedia

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

Mechanism
Mechanism

Lithium Hexamethyldisilazide-Mediated Enolization of Acylated  Oxazolidinones: Solvent, Cosolvent, and Isotope Effects on Competi
Lithium Hexamethyldisilazide-Mediated Enolization of Acylated Oxazolidinones: Solvent, Cosolvent, and Isotope Effects on Competi

LiHMDS‐Mediated Deprotonative Coupling of Toluenes with Ketones - Shigeno -  Chemistry – A European Journal - Wiley Online Library
LiHMDS‐Mediated Deprotonative Coupling of Toluenes with Ketones - Shigeno - Chemistry – A European Journal - Wiley Online Library

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

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

Scheme 2. LiHMDS mediated transesterification of benzoate esters. |  Download Scientific Diagram
Scheme 2. LiHMDS mediated transesterification of benzoate esters. | Download Scientific Diagram

Lithium bis(trimethylsilyl)amide | C6H18LiNSi2 - PubChem
Lithium bis(trimethylsilyl)amide | C6H18LiNSi2 - PubChem

File:LiHMDS.png - Wikimedia Commons
File:LiHMDS.png - Wikimedia Commons

Hexamethyldisilazane Lithium (LiHMDS)-Promoted Hydroboration of Alkynes and  Alkenes with Pinacolborane | The Journal of Organic Chemistry
Hexamethyldisilazane Lithium (LiHMDS)-Promoted Hydroboration of Alkynes and Alkenes with Pinacolborane | The Journal of Organic Chemistry

Lithium bis(trimethylsilyl)amide - Wikipedia
Lithium bis(trimethylsilyl)amide - Wikipedia

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

Organic Syntheses Procedure
Organic Syntheses Procedure

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

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