116145-60-9Relevant academic research and scientific papers
Structural exploration of cinnamate-based phosphonic acids as inhibitors of bacterial ureases
Ntatsopoulos, Vassilis,Macegoniuk, Katarzyna,Mucha, Artur,Vassiliou, Stamatia,Berlicki, ?ukasz
, p. 307 - 316 (2018)
The conjugated system of cinnamic acid, α-substituted with a phosphonoalkyl residue, was previously validated as a scaffold that provided one of the most potent organophosphorus inhibitors of bacterial urease. Following the idea of using Morita-Baylis-Hil
Stereospecific synthesis of highly substituted skipped dienes through multifunctional palladium catalysis
Thadani, Avinash N.,Rawal, Viresh H.
, p. 4317 - 4320 (2007/10/03)
(equation presented) Multifunctional palladium catalysis is utilized in the one-pot stereocontrolled synthesis of tetrasubstituted alkenes. The homogeneous palladium dihalide catalyst utilized for bromo-/chloroallylation of alkynes is then reused in situ
POLARIZED KETENE DITHIOACETALS 63. STEREOSELECTIVE SYNTHESIS OF Α-YLIDENE-Γ-BUTYROLACTONES
Datta, Apurba,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar
, p. 5367 - 5374 (2007/10/02)
A facile method for highly stereoselective synthesis of α-arylidene (4a-d, 4f-h and 4j) and α-ethylidene (4e,4i)-γ-butyrolactones has been developed by acid catalyzed lactonization of the corresponding α-ylidene-γ,δ-unsaturated esters 3a-j.The required es
