Brønsted base-catalyzed 1,2-addition/[1,2]-phospha-Brook rearrangement sequence providing functionalized phosphonates - Organic & Biomolecular Chemistry (RSC Publishing)
![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](https://pubs.rsc.org/image/article/2006/CC/b606056k/b606056k-f1.gif)
Phosphazene base-catalyzed condensation of trimethylsilylacetate with carbonyl compounds - Chemical Communications (RSC Publishing) DOI:10.1039/B606056K
![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](https://pubs.acs.org/cms/10.1021/acs.orglett.5b01648/asset/images/medium/ol-2015-01648m_0001.gif)
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
![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](https://onlinelibrary.wiley.com/cms/asset/8d307dde-94b3-4266-9dd3-2fbd42ebce38/bkcs12070-fig-0002-m.jpg)
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
The phosphazene bases P 2-Et and P 4-tBu A more successful approach has... | Download Scientific Diagram
![Organocatalytic Stereoselective Ring-Opening Polymerization of Lactide with Dimeric Phosphazene Bases | Journal of the American Chemical Society Organocatalytic Stereoselective Ring-Opening Polymerization of Lactide with Dimeric Phosphazene Bases | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja074131c/asset/images/medium/ja074131ch00001.gif)
Organocatalytic Stereoselective Ring-Opening Polymerization of Lactide with Dimeric Phosphazene Bases | Journal of the American Chemical Society
![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](https://pubs.acs.org/cms/10.1021/acs.orglett.5b01648/asset/images/large/ol-2015-01648m_0003.jpeg)
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. | Semantic Scholar P2Et Phosphazene: A Mild, Functional Group Tolerant Base for Soluble, Room Temperature Pd-Catalyzed C-N, C-O, and C-C Cross-Coupling Reactions. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/28f2e9be179769a18c466aed2bb243252b04bb2e/2-Table1-1.png)
P2Et Phosphazene: A Mild, Functional Group Tolerant Base for Soluble, Room Temperature Pd-Catalyzed C-N, C-O, and C-C Cross-Coupling Reactions. | Semantic Scholar
![Bifunctional phosphazene-thiourea/urea catalyzed ring-opening polymerization of cyclic esters - ScienceDirect Bifunctional phosphazene-thiourea/urea catalyzed ring-opening polymerization of cyclic esters - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2352492819311389-ga1.jpg)