Phosphazene base promoted anionic polymerization of n-butyraldehyde - ScienceDirect
Phosphazene base P2-F | C12H36FN7P2 | ChemSpider
Phosphazene - Wikipedia
Phosphazene base P1-t-Oct | C14H35N4P | CID 5069241 - PubChem
Polymerization Using Phosphazene Bases | SpringerLink
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
Scheme 1. Chemical structures of the phosphazene bases t-BuP1, t-BuP2... | Download Scientific Diagram
Phosphazene base P2-Et | CAS 165535-45-5 | SCBT - Santa Cruz Biotechnology
Phosphazene base P4-t-Bu solution | CAS 111324-04-0 | SCBT - Santa Cruz Biotechnology
Phosphazene Bases
Phosphazene base P2-Et | C12H35N7P2 | CID 3393106 - PubChem
31 P { 1 H} NMR spectra of the pure (a) phosphazene base 2d and (b) PIL... | 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
Phosphazene base P1-t-Bu ≥97.0% (GC) | 81675-81-2
Structure of a trimeric phosphazene base (CTPB) (adapted with... | Download Scientific Diagram
Phosphazene base-catalyzed intramolecular cyclization for efficient synthesis of benzofurans viacarbon–carbon bond formation - Chemical Communications (RSC Publishing)
Phosphazene base promoted anionic polymerization of n-butyraldehyde - ScienceDirect
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
pK ip values of phosphazene bases 6a,b and several other representative... | Download Scientific Diagram
Polymerization of epoxide monomers promoted by tBuP4 phosphazene base: a comparative study of kinetic behavior - Polymer Chemistry (RSC Publishing)
Phosphazene - Wikipedia
Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0
