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

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

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

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

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-Catalyzed Intramolecular Hydroamidation of Alkenes with  Amides | Organic Letters
Phosphazene Base-Catalyzed Intramolecular Hydroamidation of Alkenes with Amides | Organic Letters

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)

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

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

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

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

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

Phosphazene - Wikipedia
Phosphazene - Wikipedia

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

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

Phosphazene Bases
Phosphazene Bases

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

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

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

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-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

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

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