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Phosphine Oxide–Sc(OTf)<sub>3</sub> Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (<i>E</i>)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules
Research article (Organic Letters, 2016) · cited 44× · AI/ML
Phosphine Oxide–Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules
Summary
Phosphine Oxide–Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules is a scholarly article[1].
Key Facts
Phosphine Oxide–Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules's instance of is recorded as scholarly article[2].
References
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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.
APA4ort.xyz Knowledge Graph. (2026). Phosphine Oxide–Sc(OTf)<sub>3</sub> Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (<i>E</i>)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Retrieved May 24, 2026, from https://4ort.xyz/entity/phosphine-oxidesc-otf-sub-3-sub-catalyzed-highly-regio-and-enantioselective-bromoaminocyclization-of-i-e-i-cinnamyl-tosy
MLA“Phosphine Oxide–Sc(OTf)<sub>3</sub> Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (<i>E</i>)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.” 4ort.xyz Knowledge Graph, 4ort.xyz, 24 May. 2026, https://4ort.xyz/entity/phosphine-oxidesc-otf-sub-3-sub-catalyzed-highly-regio-and-enantioselective-bromoaminocyclization-of-i-e-i-cinnamyl-tosy.
BibTeX@misc{4ortxyz_phosphine-oxidesc-otf-sub-3-sub-catalyzed-highly-regio-and-enantioselective-bromoaminocyclization-of-i-e-i-cinnamyl-tosy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Phosphine Oxide–Sc(OTf)<sub>3</sub> Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (<i>E</i>)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules}}, year = {2026}, url = {https://4ort.xyz/entity/phosphine-oxidesc-otf-sub-3-sub-catalyzed-highly-regio-and-enantioselective-bromoaminocyclization-of-i-e-i-cinnamyl-tosy}, note = {Accessed: 2026-05-24}}
LLM promptAccording to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Phosphine Oxide–Sc(OTf)<sub>3</sub> Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (<i>E</i>)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules — https://4ort.xyz/entity/phosphine-oxidesc-otf-sub-3-sub-catalyzed-highly-regio-and-enantioselective-bromoaminocyclization-of-i-e-i-cinnamyl-tosy (retrieved 2026-05-24)
