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Philosophique Tremplin débutant phosphazene base étiquette pastille g

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

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

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

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

Phosphazene base P1-t-Bu-tris(tetramethylene) | CAS 161118-67-8 | SCBT -  Santa Cruz Biotechnology
Phosphazene base P1-t-Bu-tris(tetramethylene) | CAS 161118-67-8 | SCBT - Santa Cruz Biotechnology

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

Polymerization Using Phosphazene Bases | SpringerLink
Polymerization Using Phosphazene Bases | SpringerLink

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

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

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

Phosphazene base P1-t-Bu ≥97.0% (GC) | 81675-81-2
Phosphazene base P1-t-Bu ≥97.0% (GC) | 81675-81-2

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

Anionic ring‐opening polymerization of N‐glycidylphthalimide: Combination  of phosphazene base and activated monomer mechanism - Rassou - 2018 -  Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library
Anionic ring‐opening polymerization of N‐glycidylphthalimide: Combination of phosphazene base and activated monomer mechanism - Rassou - 2018 - Journal of Polymer Science Part A: Polymer Chemistry - 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

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

Phosphazene bases
Phosphazene bases

Phosphazene - Wikipedia
Phosphazene - Wikipedia

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)

2-tert-Butylamino-1-methyl-2-[tris(dimethylamino)phosphoranylidenamino]-perhydro-1,3,2-diazaphosphorinium  iodide purum, ≥97.0% (CHN) | Sigma-Aldrich
2-tert-Butylamino-1-methyl-2-[tris(dimethylamino)phosphoranylidenamino]-perhydro-1,3,2-diazaphosphorinium iodide purum, ≥97.0% (CHN) | Sigma-Aldrich

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

Polymerization of epoxide monomers promoted by tBuP4 phosphazene base: a  comparative study of kinetic behavior - Polymer Chemistry (RSC Publishing)
Polymerization of epoxide monomers promoted by tBuP4 phosphazene base: a comparative study of kinetic behavior - Polymer Chemistry (RSC Publishing)

Phosphazene base-catalyzed condensation of trimethylsilylacetate with  carbonyl compounds - Chemical Communications (RSC Publishing)  DOI:10.1039/B606056K
Phosphazene base-catalyzed condensation of trimethylsilylacetate with carbonyl compounds - Chemical Communications (RSC Publishing) DOI:10.1039/B606056K

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

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 Bases
Phosphazene Bases