Scheme 55. Reagents: i, LiHMDS, THF, –78ºC; ii, oiodobenzaldehyde ;... | Download Scientific Diagram
Scheme 2. LiHMDS mediated transesterification of benzoate esters. | Download Scientific Diagram
Scheme5.Reagents and conditions: a) 13,LiHMDS, THF, À78 8C; then add... | Download Scientific Diagram
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
Organic Syntheses Procedure
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition - ScienceDirect
Lithium bis(trimethylsilyl)amide - Wikipedia
Chemjobber: Process Wednesday: a LiHMDS mystery
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
Highly selective transition-metal-free transamidation of amides and amidation of esters at room temperature | Nature Communications
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
Reaction of Ketones with Lithium Hexamethyldisilazide: Competitive Enolizations and 1,2-Additions | Journal of the American Chemical Society
Lithium Hexamethyldisilazide-Mediated Enolization of Acylated Oxazolidinones: Solvent, Cosolvent, and Isotope Effects on Competi
Lithium bis(trimethylsilyl)amide | C6H18LiNSi2 - PubChem
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 Acylated Oxazolidinones: Solvent, Cosolvent, and Isotope Effects on Competi
Lithium hexamethyldisilazide initiated superfast ring opening polymerization of alpha-amino acid N-carboxyanhydrides | Nature Communications
Mechanism
Lithium bis(trimethylsilyl)amide - Wikipedia
