Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0
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
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
31 P { 1 H} NMR spectra of the pure (a) phosphazene base 2d and (b) PIL... | Download Scientific Diagram
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
Phosphazene - Wikipedia
PHOSPHAZENE BASE P1-T-BU | 81675-81-2
Phosphazene base P2-Et = 98.0 NT 165535-45-5
Phosphazene base P1-t-Oct | C14H35N4P | CID 5069241 - PubChem
Phosphazene base P4-t-Bu | C22H63N13P4 | ChemSpider
Scheme 1. Chemical structures of the phosphazene bases t-BuP1, t-BuP2... | Download Scientific Diagram
Phosphazene base-catalyzed condensation of trimethylsilylacetate with carbonyl compounds - Chemical Communications (RSC Publishing) DOI:10.1039/B606056K
Phosphazene base P2-Et | C12H35N7P2 | CID 3393106 - PubChem
Phosphazene base P1-t-Bu ≥97.0% (GC) | 81675-81-2
Two-Step Asymmetric Synthesis of Disubstituted N-Tosyl Aziridines Having 98−100% ee: Use of a Phosphazene Base | The Journal of Organic Chemistry
Polymerization of epoxide monomers promoted by tBuP4 phosphazene base: a comparative study of kinetic behavior - Polymer Chemistry (RSC Publishing)
Phosphazene Base-Catalyzed Intramolecular Hydroamidation of Alkenes with Amides | Organic Letters
Phosphazene base promoted anionic polymerization of n-butyraldehyde - ScienceDirect
Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0
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
