Home

voyelle contribution Persée verkade base La source Parolier marqueur

Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the  Catalytic Dimerization of Alkynes | Organometallics
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics

Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile  Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations |  Inorganic Chemistry
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry

Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile  Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations |  Inorganic Chemistry
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry

Verkade's base | C6H15N4P - PubChem
Verkade's base | C6H15N4P - PubChem

Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile  Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations |  Inorganic Chemistry
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry

Protonation of Verkade bases: a theoretical study - New Journal of  Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G
Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G

Kees Verkade (1941-2020) Sculptures for Sale
Kees Verkade (1941-2020) Sculptures for Sale

Protonation of Verkade bases: a theoretical study - New Journal of  Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G
Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G

Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the  Catalytic Dimerization of Alkynes | Organometallics
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics

Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile  Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations |  Inorganic Chemistry
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry

Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the  Catalytic Dimerization of Alkynes | Organometallics
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics

Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile  Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations |  Inorganic Chemistry
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry

Acids & Bases
Acids & Bases

Bridge in d minor (extended mix) | Karl Verkade
Bridge in d minor (extended mix) | Karl Verkade

Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the  Catalytic Dimerization of Alkynes | Organometallics
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics

Verkade base - Wikipedia
Verkade base - Wikipedia

Two Verkade's super bases (Vkd_Me and Vkd_iPr) and two guanidine bases... |  Download Scientific Diagram
Two Verkade's super bases (Vkd_Me and Vkd_iPr) and two guanidine bases... | Download Scientific Diagram

Protonation of Verkade bases: a theoretical study - New Journal of  Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G
Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G

Figure 1 from Very strong organosuperbases formed by combining imidazole  and guanidine bases: synthesis, structure, and basicity. | Semantic Scholar
Figure 1 from Very strong organosuperbases formed by combining imidazole and guanidine bases: synthesis, structure, and basicity. | Semantic Scholar

Lot - Kees Verkade, (b. 1941 Dutch), Two figures perfoming handstands,  1969, Patinated bronze on white marble base, Bronze: 11" H x 11" W x 8
Lot - Kees Verkade, (b. 1941 Dutch), Two figures perfoming handstands, 1969, Patinated bronze on white marble base, Bronze: 11" H x 11" W x 8

Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile  Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations |  Inorganic Chemistry
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry

Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the  Catalytic Dimerization of Alkynes | Organometallics
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics

Protonation of Verkade bases: a theoretical study - New Journal of  Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G
Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G

Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the  Catalytic Dimerization of Alkynes | Organometallics
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics