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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

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

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

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

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

Organic Syntheses Procedure
Organic Syntheses Procedure

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

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

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

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

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 bis(trimethylsilyl)amide - Wikiwand
Lithium bis(trimethylsilyl)amide - Wikiwand

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

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

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

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

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