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Cercle Lundi clé phosphazene base p2 et prise de courant orateur gène

165535-45-5|Phosphazene base P2-Et|Sigma Aldrich|1-乙基-2,2,4,4,4-五(二甲氨基)-...
165535-45-5|Phosphazene base P2-Et|Sigma Aldrich|1-乙基-2,2,4,4,4-五(二甲氨基)-...

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

Phosphazene base P2-Et
Phosphazene base P2-Et

The phosphazene bases P 2-Et and P 4-tBu A more successful approach has...  | Download Scientific Diagram
The phosphazene bases P 2-Et and P 4-tBu A more successful approach has... | Download Scientific Diagram

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

Phosphazene Cations | Inorganic Chemistry
Phosphazene Cations | Inorganic Chemistry

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

Phosphazene base P2-t-Bu on polystyrene extent of labeling: ~1.6 mmol/g  loading | Sigma-Aldrich
Phosphazene base P2-t-Bu on polystyrene extent of labeling: ~1.6 mmol/g loading | Sigma-Aldrich

Examples of phosphazene structures. | Download Scientific Diagram
Examples of phosphazene structures. | 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

Bifunctional phosphazene-thiourea/urea catalyzed ring-opening  polymerization of cyclic esters - ScienceDirect
Bifunctional phosphazene-thiourea/urea catalyzed ring-opening polymerization of cyclic esters - 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
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 P2-t-Bu solution | CAS 111324-03-9 | SCBT - Santa Cruz  Biotechnology
Phosphazene base P2-t-Bu solution | CAS 111324-03-9 | SCBT - Santa Cruz Biotechnology

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

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 Bases
Phosphazene Bases

1,1,1,3,3,3-Hexakis(dimethylamino)diphosphazenium tetrafluoroborate = 98.0  T 137334-98-6
1,1,1,3,3,3-Hexakis(dimethylamino)diphosphazenium tetrafluoroborate = 98.0 T 137334-98-6

Phosphazene base P2-t-Bu 2.0M tetrahydrofuran 111324-03-9
Phosphazene base P2-t-Bu 2.0M tetrahydrofuran 111324-03-9

Phosphazene base P2-F | C12H36FN7P2 | ChemSpider
Phosphazene base P2-F | C12H36FN7P2 | ChemSpider

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

A Successful Application of Phosphazene Base P2‐tBu to [11C]ABP688  Radiosynthesis in Fully Automated Synthesis Module - Lee - 2020 - Bulletin  of the Korean Chemical Society - Wiley Online Library
A Successful Application of Phosphazene Base P2‐tBu to [11C]ABP688 Radiosynthesis in Fully Automated Synthesis Module - Lee - 2020 - Bulletin of the Korean Chemical Society - Wiley Online Library

Phosphazene base P4-t-Bu 0.8M hexane 111324-04-0
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
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-promoted halogen –zinc exchange reaction of aryl iodides  using diethylzinc - Chemical Communications (RSC Publishing)  DOI:10.1039/B605807H
Phosphazene base-promoted halogen –zinc exchange reaction of aryl iodides using diethylzinc - Chemical Communications (RSC Publishing) DOI:10.1039/B605807H