61076-91-3Relevant academic research and scientific papers
9-Phenylfluorene: A powerful labeling agent
Cintrat, Jean-Christophe,Pillon, Florence,Rousseau, Bernard
, p. 5001 - 5003 (2001)
A highly efficient method for labeling with deuterium is described using an acidic hydrocarbon as transfer agent. Using 9-[2H]-9-phenylfluorene as the deuterium donor, numerous organic compounds have been labeled in fair yields and good isotopic enrichment.
Room-Temperature Palladium-Catalyzed Deuterogenolysis of Carbon Oxygen Bonds towards Deuterated Pharmaceuticals
Ou, Wei,Xiang, Xudong,Zou, Ru,Xu, Qing,Loh, Kian Ping,Su, Chenliang
supporting information, p. 6357 - 6361 (2021/02/16)
Site-specific incorporation of deuterium into drug molecules to study and improve their biological properties is crucial for drug discovery and development. Herein, we describe a palladium-catalyzed room-temperature deuterogenolysis of carbon–oxygen bonds
KHMDS mediated synthesis of 9-arylfluorenes from dibenzothiophene dioxides and arylacetonitriles by tandem SNAr-decyanation-based arylation
Mylavarapu, Saketh,Yadav, Mamta,Bhanuchandra
, p. 7815 - 7819 (2018/11/21)
A straightforward KHMDS mediated synthetic route to 9-arylfluorenes from readily available starting materials has been developed. This reaction involves SNAr reactions of dioxide with arylacetonitriles, followed by decyanation reaction. The pro
Classical Organic Reactions in Pure Superheated Water
Kuhlmann, Barbara,Arnett, Edward M.,Siskin, Michael
, p. 3098 - 3101 (2007/10/02)
At high temperatures and pressures, pure liquid water becomes a surprisingly effective medium for the reactions of organic compounds.It may function simultaneously as a convenient solvent, catalyst, and reagent for reactions which are typically acid- or base-catalyzed.Rapid and highly selective conversion are observed for the majority of the compounds in this study.
