351981-71-0Relevant academic research and scientific papers
Potential bioactive Schiff base compounds: Synthesis, characterization, X-ray structures, biological screenings and interaction with Salmon sperm DNA
Sirajuddin, Muhammad,Uddin, Noor,Ali, Saqib,Tahir, Muhammad Nawaz
, p. 111 - 121 (2013)
(Figure Presented) Three Schiff base compounds of N′-substituted benzohydrazide and sulfonohydrazide derivatives: N′-(2-hydroxy-3- methoxybenzylidene)-4-tert-butyl- benzohydrazide (1), N′-(5-bromo-2- hydroxybenzylidene)-4-tert-butylbenzohydrazide (2) and
Enantio- and Diastereoselective, Complete Hydrogenation of Benzofurans by Cascade Catalysis
Gallagher, Timothy,Glorius, Frank,Hu, Tianjiao,Moock, Daniel,Wagener, Tobias
supporting information, p. 13677 - 13681 (2021/05/10)
We report an enantio- and diastereoselective, complete hydrogenation of multiply substituted benzofurans in a one-pot cascade catalysis. The developed protocol facilitates the controlled installation of up to six new defined stereocenters and produces architecturally complex octahydrobenzofurans, prevalent in many bioactive molecules. A unique match of a chiral homogeneous ruthenium-N-heterocyclic carbene complex and an in situ activated rhodium catalyst from a complex precursor act in sequence to enable the presented process.
Palladium-catalyzed coupling of N-tosylhydrazones and β-bromostyrene derivatives: New approach to 2H-chromenes
Xia, Yamu,Xia, Ying,Zhang, Yan,Wang, Jianbo
supporting information, p. 9333 - 9336 (2014/12/11)
2H-Chromene is an important structural motif that exists in natural products and non-natural compounds possessing interesting biological activities. In this investigation, a highly efficient approach toward 2H-chromenes has been developed based on palladium-catalyzed coupling of N-tosylhydrazones and β-bromostyrenes. The mechanism of this reaction is proposed that involves the formation of vinyl palladium by carbene migratory insertion and the intramolecular nucleophilic substitution. This journal is
