80335-80-4Relevant academic research and scientific papers
Reactions of (Z)-3-aryl-3-chloropropenals with nucleophiles: Stereoselective formation of (E)-vinylogous esters, (E)-vinylogous amides, and vinamidinium salts
Clough, Stuart,Gupton, John,Ligali, Adepeju,Roberts, Matthew,Driscoll, David,Annett, Scott,Hewitt, Alisa,Hudson, Matthew,Jackson, Edward,Miller, Robert,Norwood, Bradley,Kanters, Rene,Wyre, Hadley,Petruzzi, Heather
, p. 7554 - 7561 (2007/10/03)
The highly stereoselective conversions of (Z)-3-aryl-3-chloropropenals to (E)-3-alkoxy-3-arylpropenals, to (E)-3-aryl-3-morphorlinopropenals, and to vinamidinium salts are reported. The stereochemical assignments were based on 2D-NMR experiments.
Nonpeptide Angiotensin II Receptor Antagonists. Synthesis, in Vitro Activity, and Molecular Modeling Studies of N-imidazoles
Salimbeni, Aldo,Canevotti, Renato,Paleari, Fabio,Bonaccorsi, Fabrizio,Renzetti, Anna R.,et al.
, p. 3928 - 3938 (2007/10/02)
With the aim of explaining the influence of the structural changes on the biphenylic moiety on the activity, a series of N-imidazoles (I), constructed on the model of DuPont compounds by replacing either the central or terminal pheny
