Chemjobber: Process Wednesday: a LiHMDS mystery
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
Mechanism
LiHMDS‐Mediated Deprotonative Coupling of Toluenes with Ketones - Shigeno - Chemistry – A European Journal - Wiley Online Library
Solved LiHMDS, FCIO3 THF, -40 °C Fclosa e | Chegg.com
Lithium bis(trimethylsilyl)amide - Wikipedia
Scheme5.Reagents and conditions: a) 13,LiHMDS, THF, À78 8C; then add... | Download Scientific Diagram
File:LiHMDS.png - Wikimedia Commons
Scheme 15. Synthesis of AM281 (74). Reagents and conditions: (a) (i)... | Download Scientific Diagram
Lithium bis(trimethylsilyl)amide - Wikipedia
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
Lithium Hexamethyldisilazide-Mediated Enolization of Highly Substituted Aryl Ketones: Structural and Mechanistic Basis of the E/Z Selectivities. - Abstract - Europe PMC
Reaction of Ketones with Lithium Hexamethyldisilazide: Competitive Enolizations and 1,2-Additions | Journal of the American Chemical Society
Lithium bis(trimethylsilyl)amide - Wikipedia
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
Scheme 2. LiHMDS mediated transesterification of benzoate esters. | Download Scientific Diagram
