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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

Schwesinger P4 Base-Molbase
Schwesinger P4 Base-Molbase

Dr. Kathrin Schwesinger | Associate | White & Case LLP
Dr. Kathrin Schwesinger | Associate | White & Case LLP

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

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

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

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

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

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

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

Phosphazene Bases
Phosphazene Bases

Phosphazene - Wikipedia
Phosphazene - Wikipedia

Deployed wing contributes aircraft, Airmen to relief efforts in Pakistan >  Air Mobility Command > Article Display
Deployed wing contributes aircraft, Airmen to relief efforts in Pakistan > Air Mobility Command > Article Display

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

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

Heredity and Environment in Man: "Heredity and Environment: Studies in the  Genesis of Psychological Characteristics," by Gladys C. Schwesinger. (Ed.  by Frederick Osborn), 479 pp. N. Y.: Macmillan, 1933. $4.00. | Science
Heredity and Environment in Man: "Heredity and Environment: Studies in the Genesis of Psychological Characteristics," by Gladys C. Schwesinger. (Ed. by Frederick Osborn), 479 pp. N. Y.: Macmillan, 1933. $4.00. | Science

How Strong and How Hindered Can Uncharged Phosphazene Bases Be? -  Schwesinger - 1993 - Angewandte Chemie International Edition in English -  Wiley Online Library
How Strong and How Hindered Can Uncharged Phosphazene Bases Be? - Schwesinger - 1993 - Angewandte Chemie International Edition in English - Wiley Online Library

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 P2-t-Bu solution | CAS 111324-03-9 | SCBT - Santa Cruz  Biotechnology
Phosphazene base P2-t-Bu solution | CAS 111324-03-9 | SCBT - Santa Cruz Biotechnology

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

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

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

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

Schwesinger P4 Base
Schwesinger P4 Base

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

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

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

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

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

Acids & Bases
Acids & Bases