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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

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

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

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

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

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

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

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

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
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect

Regiospecificity in Ligand-Free Pd-Catalyzed C–H Arylation of Indoles:  LiHMDS as Base and Transient Directing Group | ACS Catalysis
Regiospecificity in Ligand-Free Pd-Catalyzed C–H Arylation of Indoles: LiHMDS as Base and Transient Directing Group | ACS Catalysis

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

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

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

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

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

Organic Syntheses Procedure
Organic Syntheses Procedure