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Phosphazene base P1-t-Bu-tris(tetramethylene) = 97.0 NT 161118-67-8
Phosphazene base P1-t-Bu-tris(tetramethylene) = 97.0 NT 161118-67-8

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

Phosphazene Bases
Phosphazene Bases

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

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

Phosphazene Bases
Phosphazene Bases

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

Deprotonation of benzylic ethers using a hindered phosphazene base. A  synthesis of benzofurans from ortho-substituted benzaldehydes. | Semantic  Scholar
Deprotonation of benzylic ethers using a hindered phosphazene base. A synthesis of benzofurans from ortho-substituted benzaldehydes. | Semantic Scholar

Phosphazene base-promoted functionalization of aryltrimethylsilanes -  Chemical Communications (RSC Publishing) DOI:10.1039/B611090H
Phosphazene base-promoted functionalization of aryltrimethylsilanes - Chemical Communications (RSC Publishing) DOI:10.1039/B611090H

Phosphazene base P2-Et | C12H35N7P2 | ChemSpider
Phosphazene base P2-Et | C12H35N7P2 | ChemSpider

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

Scheme 1. Chemical structures of the phosphazene bases t-BuP1, t-BuP2... |  Download Scientific Diagram
Scheme 1. Chemical structures of the phosphazene bases t-BuP1, t-BuP2... | Download Scientific Diagram

Phosphazene base P1-tert-butyl- tris(tetramethylene) - ATR-IR - Spectrum -  SpectraBase
Phosphazene base P1-tert-butyl- tris(tetramethylene) - ATR-IR - Spectrum - SpectraBase

CAS#:111324-04-0 | Phosphazene base P4-t-Bu solution purum, ~1.0 M in  hexane | Chemsrc
CAS#:111324-04-0 | Phosphazene base P4-t-Bu solution purum, ~1.0 M in hexane | Chemsrc

Phosphazene base P2-t-Bu on polystyrene extent of labeling: ~1.6 mmol/g  loading | Sigma-Aldrich
Phosphazene base P2-t-Bu on polystyrene extent of labeling: ~1.6 mmol/g loading | Sigma-Aldrich

Phosphazene | Phosphazene base |Structure of phosphazene |Inorganic  Chemistry|MSc.1st semester notes - YouTube
Phosphazene | Phosphazene base |Structure of phosphazene |Inorganic Chemistry|MSc.1st semester notes - YouTube

Phosphazene - Wikipedia
Phosphazene - Wikipedia

Phosphazene base P4-t-Bu tetrafluoroborate salt ≥97.0% (NMR) | Sigma-Aldrich
Phosphazene base P4-t-Bu tetrafluoroborate salt ≥97.0% (NMR) | Sigma-Aldrich

Phosphazene - Wikipedia
Phosphazene - Wikipedia

Phosphazene base P4-t-Oct 1.00M +/- 0.05M n-hexane 153136-05-1
Phosphazene base P4-t-Oct 1.00M +/- 0.05M n-hexane 153136-05-1

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-Et - ATR-IR - Spectrum - SpectraBase
Phosphazene base P2-Et - ATR-IR - Spectrum - SpectraBase

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)