Home

Élucidation Observatoire Spirituel phosphazene base conducteur appel Comparable

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

Phosphazene Bases
Phosphazene Bases

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

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 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

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

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

Phosphazene Bases
Phosphazene Bases

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

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

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

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

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

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

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

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

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

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 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-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 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