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Sigma Aldrich Fine Chemicals Biosciences PHOSPHAZENE BASE P4-T-BU SOLUT, |  Fisher Scientific
Sigma Aldrich Fine Chemicals Biosciences PHOSPHAZENE BASE P4-T-BU SOLUT, | Fisher Scientific

pK ip values of phosphazene bases 6a,b and several other representative...  | Download Scientific Diagram
pK ip values of phosphazene bases 6a,b and several other representative... | Download Scientific Diagram

Phosphazene base P2-Et | CAS 165535-45-5 | SCBT - Santa Cruz Biotechnology
Phosphazene base P2-Et | CAS 165535-45-5 | SCBT - Santa Cruz Biotechnology

Phosphazene Base tBu‐P4 Catalyzed Methoxy–Alkoxy Exchange Reaction on  (Hetero)Arenes - Shigeno - 2019 - Chemistry – A European Journal -  Wiley Online Library
Phosphazene Base tBu‐P4 Catalyzed Methoxy–Alkoxy Exchange Reaction on (Hetero)Arenes - Shigeno - 2019 - Chemistry – A European Journal - Wiley Online Library

Structural Effect of Organic Catalytic Pairs Based on Chiral  Amino(thio)ureas and Phosphazene Bases for the Isoselective Ring-Opening  Polymerization of Racemic Lactide | Macromolecules
Structural Effect of Organic Catalytic Pairs Based on Chiral Amino(thio)ureas and Phosphazene Bases for the Isoselective Ring-Opening Polymerization of Racemic Lactide | Macromolecules

Phosphazene base-catalyzed intramolecular cyclization for efficient  synthesis of benzofurans viacarbon–carbon bond formation - Chemical  Communications (RSC Publishing)
Phosphazene base-catalyzed intramolecular cyclization for efficient synthesis of benzofurans viacarbon–carbon bond formation - Chemical Communications (RSC Publishing)

Phosphazene Bases
Phosphazene Bases

PHOSPHAZENE BASE P1-T-BU | 81675-81-2
PHOSPHAZENE BASE P1-T-BU | 81675-81-2

Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0
Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0

Phosphazene Bases
Phosphazene Bases

Structure of a trimeric phosphazene base (CTPB) (adapted with... | Download  Scientific Diagram
Structure of a trimeric phosphazene base (CTPB) (adapted with... | Download Scientific Diagram

Phosphazene base P2-F | C12H36FN7P2 | ChemSpider
Phosphazene base P2-F | C12H36FN7P2 | ChemSpider

Phosphazene base P2-Et = 98.0 NT 165535-45-5
Phosphazene base P2-Et = 98.0 NT 165535-45-5

Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0
Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0

Phosphazene bases
Phosphazene bases

P2Et Phosphazene: A Mild, Functional Group Tolerant Base for Soluble, Room  Temperature Pd-Catalyzed C–N, C–O, and C–C Cross-Coupling Reactions |  Organic Letters
P2Et Phosphazene: A Mild, Functional Group Tolerant Base for Soluble, Room Temperature Pd-Catalyzed C–N, C–O, and C–C Cross-Coupling Reactions | Organic Letters

Phosphazene base P2-Et | C12H35N7P2 | CID 3393106 - PubChem
Phosphazene base P2-Et | C12H35N7P2 | CID 3393106 - PubChem

Phosphazene base P1-t-Oct | C14H35N4P | CID 5069241 - PubChem
Phosphazene base P1-t-Oct | C14H35N4P | CID 5069241 - PubChem

31 P { 1 H} NMR spectra of the pure (a) phosphazene base 2d and (b) PIL...  | Download Scientific Diagram
31 P { 1 H} NMR spectra of the pure (a) phosphazene base 2d and (b) PIL... | Download Scientific Diagram

Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0
Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0

Phosphazene base promoted anionic polymerization of n-butyraldehyde -  ScienceDirect
Phosphazene base promoted anionic polymerization of n-butyraldehyde - ScienceDirect

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

Two-Step Asymmetric Synthesis of Disubstituted N-Tosyl Aziridines Having  98−100% ee: Use of a Phosphazene Base | The Journal of Organic Chemistry
Two-Step Asymmetric Synthesis of Disubstituted N-Tosyl Aziridines Having 98−100% ee: Use of a Phosphazene Base | The Journal of Organic Chemistry