Phosphazene Bases
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
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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
Schwesinger P4 Base
How Strong and How Hindered Can Uncharged Phosphazene Bases Be? - Schwesinger - 1993 - Angewandte Chemie International Edition in English - Wiley Online Library
P4-t-Bu - Wikipedia
The structure of the base t-Bu-P4 and its protonated form. | Download Scientific Diagram
P4-t-Bu - Wikipedia
Angewandte Chemie on Twitter: "Stable Singlet Carbenes as Organic Superbases (Bertrand) @UCSDChemBiochem @Rodolphe_Jazzar https://t.co/1KmUvGHY5h https://t.co/fiCQLQojAV" / Twitter
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
Total Synthesis of Coraxeniolide A by Corey
Dr. Kathrin Schwesinger | Associate | White & Case LLP
Phosphazene - Wikipedia
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
Mechanistic Studies Yield Improved Protocols for Base-Catalyzed Anti-Markovnikov Alcohol Addition Reactions | Journal of the American Chemical Society
Polymerization Using Phosphazene Bases | SpringerLink
Phosphazene base P4-t-Bu | C22H63N13P4 | ChemSpider
Phosphazene base-catalyzed hydroamination of aminoalkenes for the construction of isoindoline scaffolds: Application to the total synthesis of aristocularine - ScienceDirect
P4-t-Bu - Wikipedia
