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The structure of the base t-Bu-P4 and its protonated form. | Download  Scientific Diagram
The structure of the base t-Bu-P4 and its protonated form. | Download Scientific Diagram

IJMS | Free Full-Text | Modeling pKa of the Brønsted Bases as an  Approach to the Gibbs Energy of the Proton in Acetonitrile
IJMS | Free Full-Text | Modeling pKa of the Brønsted Bases as an Approach to the Gibbs Energy of the Proton in Acetonitrile

Higher-Order Cyclopropenimine Superbases: Direct Neutral Brønsted Base  Catalyzed Michael Reactions with α-Aryl Esters | Journal of the American  Chemical Society
Higher-Order Cyclopropenimine Superbases: Direct Neutral Brønsted Base Catalyzed Michael Reactions with α-Aryl Esters | Journal of the American Chemical Society

Higher-Order Cyclopropenimine Superbases: Direct Neutral Brønsted Base  Catalyzed Michael Reactions with α-Aryl Esters | Journal of the American  Chemical Society
Higher-Order Cyclopropenimine Superbases: Direct Neutral Brønsted Base Catalyzed Michael Reactions with α-Aryl Esters | Journal of the American Chemical Society

Mono‐Phosphazenyl Phosphines (R2N)3P=N–P(NR2)2 – Strong P‐Bases, P‐Donors,  and P‐Nucleophiles for the Construction of Chelates - Kögel - 2020 -  Zeitschrift für anorganische und allgemeine Chemie - Wiley Online  Library
Mono‐Phosphazenyl Phosphines (R2N)3P=N–P(NR2)2 – Strong P‐Bases, P‐Donors, and P‐Nucleophiles for the Construction of Chelates - Kögel - 2020 - Zeitschrift für anorganische und allgemeine Chemie - Wiley Online Library

Phosphazene base-catalyzed hydroamination of aminoalkenes for the  construction of isoindoline scaffolds: Application to the total synthesis  of aristocularine - ScienceDirect
Phosphazene base-catalyzed hydroamination of aminoalkenes for the construction of isoindoline scaffolds: Application to the total synthesis of aristocularine - ScienceDirect

Schwesinger P4 Base-Molbase
Schwesinger P4 Base-Molbase

A Short Novel Synthesis of the Phosphazene Base Et-P
A Short Novel Synthesis of the Phosphazene Base Et-P

Phosphazene base P4-t-Bu | C22H63N13P4 | ChemSpider
Phosphazene base P4-t-Bu | C22H63N13P4 | ChemSpider

A New Strategy for Deprotonative Functionalization of Aromatics:  Transformations with Excellent Chemoselectivity and Unique  Regioselectivities Using t-Bu-P4 Base | Journal of the American Chemical  Society
A New Strategy for Deprotonative Functionalization of Aromatics: Transformations with Excellent Chemoselectivity and Unique Regioselectivities Using t-Bu-P4 Base | Journal of the American Chemical Society

2.12 Binding motives in some of SCHWESINGER's Px-bases. The arrangement...  | Download Scientific Diagram
2.12 Binding motives in some of SCHWESINGER's Px-bases. The arrangement... | Download Scientific Diagram

Phosphorus‐Containing Superbases: Recent Progress in the Chemistry of  Electron‐Abundant Phosphines and Phosphazenes - Weitkamp - 2021 - Chemistry  – A European Journal - Wiley Online Library
Phosphorus‐Containing Superbases: Recent Progress in the Chemistry of Electron‐Abundant Phosphines and Phosphazenes - Weitkamp - 2021 - Chemistry – A European Journal - Wiley Online Library

Phosphazene - Wikipedia
Phosphazene - Wikipedia

Acids & Bases
Acids & Bases

Stable Singlet Carbenes as Organic Superbases
Stable Singlet Carbenes as Organic Superbases

P4-t-Bu - Wikipedia
P4-t-Bu - Wikipedia

The structure of the base t-Bu-P4 and its protonated form. | Download  Scientific Diagram
The structure of the base t-Bu-P4 and its protonated form. | Download Scientific Diagram

Phosphazene base P4-t-Bu solution | CAS 111324-04-0 | SCBT - Santa Cruz  Biotechnology
Phosphazene base P4-t-Bu solution | CAS 111324-04-0 | SCBT - Santa Cruz Biotechnology

Phosphazene Bases
Phosphazene Bases

Generation and Applications of the Hydroxide Trihydrate Anion, [OH(OH2)3]−,  Stabilized by a Weakly Coordinating Cation - Weitkamp - 2019 - Angewandte  Chemie International Edition - Wiley Online Library
Generation and Applications of the Hydroxide Trihydrate Anion, [OH(OH2)3]−, Stabilized by a Weakly Coordinating Cation - Weitkamp - 2019 - Angewandte Chemie International Edition - Wiley Online Library

Intramolecular Alkene Hydroamination with Hybrid Catalysts Consisting of a  Metal Salt and a Neutral Organic Base - Stegner - 2020 - European Journal  of Inorganic Chemistry - Wiley Online Library
Intramolecular Alkene Hydroamination with Hybrid Catalysts Consisting of a Metal Salt and a Neutral Organic Base - Stegner - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library

Angewandte Chemie on Twitter: "Stable Singlet Carbenes as Organic  Superbases (Bertrand) @UCSDChemBiochem @Rodolphe_Jazzar  https://t.co/1KmUvGHY5h https://t.co/fiCQLQojAV" / Twitter
Angewandte Chemie on Twitter: "Stable Singlet Carbenes as Organic Superbases (Bertrand) @UCSDChemBiochem @Rodolphe_Jazzar https://t.co/1KmUvGHY5h https://t.co/fiCQLQojAV" / Twitter

A New Synthetic Pathway to the Second and Third Generation of Superbasic  Bisphosphazene Proton Sponges: The Run for the Best Chelating Ligand for a  Proton | Journal of the American Chemical Society
A New Synthetic Pathway to the Second and Third Generation of Superbasic Bisphosphazene Proton Sponges: The Run for the Best Chelating Ligand for a Proton | Journal of the American Chemical Society

Phosphorus‐Containing Superbases: Recent Progress in the Chemistry of  Electron‐Abundant Phosphines and Phosphazenes - Weitkamp - 2021 - Chemistry  – A European Journal - Wiley Online Library
Phosphorus‐Containing Superbases: Recent Progress in the Chemistry of Electron‐Abundant Phosphines and Phosphazenes - Weitkamp - 2021 - Chemistry – A European Journal - Wiley Online Library

Phosphazene base P4-t-Bu solution | CAS 111324-04-0 | SCBT - Santa Cruz  Biotechnology
Phosphazene base P4-t-Bu solution | CAS 111324-04-0 | SCBT - Santa Cruz Biotechnology

Mechanistic Studies Yield Improved Protocols for Base-Catalyzed  Anti-Markovnikov Alcohol Addition Reactions | Journal of the American  Chemical Society
Mechanistic Studies Yield Improved Protocols for Base-Catalyzed Anti-Markovnikov Alcohol Addition Reactions | Journal of the American Chemical Society