obișnuit lopată Vinovat phosphazene baze phosphazan Prin urmare sete citind
Phosphazene Base tBu‐P4 Catalyzed Methoxy–Alkoxy Exchange Reaction on (Hetero)Arenes - Shigeno - 2019 - Chemistry – A European Journal - Wiley Online Library
The structure of the base t-Bu-P4 and its protonated form. | Download Scientific Diagram
Polymerization of epoxide monomers promoted by tBuP4 phosphazene base: a comparative study of kinetic behavior - Polymer Chemistry (RSC Publishing)
Phosphazene-Based Ionic Liquids | IntechOpen
Synthesis of linear and star poly(ε-caprolactone) with controlled and high molecular weights via cyclic trimeric phosphazene base catalyzed ring-openi ... - Polymer Chemistry (RSC Publishing) DOI:10.1039/C7PY01673E
Phosphazene base-catalyzed hydroamination of aminoalkenes for the construction of isoindoline scaffolds: Application to the total synthesis of aristocularine - ScienceDirect
Polymers | Free Full-Text | Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines | HTML
Phosphazene - Wikipedia
Phosphazene base promoted anionic polymerization of n-butyraldehyde - ScienceDirect
Deprotonation of benzylic ethers using a hindered phosphazene base. A synthesis of benzofurans from ortho-substituted benzaldehydes. | Semantic Scholar
Phosphazene base P2-Et | C12H35N7P2 - PubChem
Polymerization Using Phosphazene Bases | SpringerLink
Phosphazene Bases
Phosphazene base promoted anionic polymerization of n-butyraldehyde - ScienceDirect
Examples of phosphazene structures. | Download Scientific Diagram
Phosphazene base P1-tert-butyl- tris(tetramethylene) - ATR-IR - Spectrum - SpectraBase
Phosphazene bases
Phosphazene base P2-Et = 98.0 NT 165535-45-5
Synthesis of Tris-Phosphazene Bases with Triazine as Core and Their Applications for Efficient Ring-Opening Alternating Copolymerization of Epoxide and Anhydride: Notable Effect of Basicity and Molecular Size | ACS Macro Letters
Phosphazene - Wikipedia
Phosphazene base P1-t-Oct = 97.0 161118-69-0
Phosphazene base-catalyzed intramolecular cyclization for efficient synthesis of benzofurans viacarbon–carbon bond formation - Chemical Communications (RSC Publishing)
Phosphazene base P4-t-Oct 1.00M +/- 0.05M n-hexane 153136-05-1
Tris(2,4,6-trimethoxyphenyl)phosphine - a Lewis base able to compete with phosphazene bases in catalysing oxa-Michael reactions | Organic Chemistry | ChemRxiv | Cambridge Open Engage