نتایج جستجو برای: aminolysis

تعداد نتایج: 308  

2013
Yizheng Jin Qing Yi Yuping Ren Xin Wang Zhizhen Ye

Molecular mechanisms and precursor conversion pathways associated with the reactions that generate colloidal nanocrystals are crucial for the development of rational synthetic protocols. In this study, Fourier transform infrared spectroscopy technique was employed to explore the molecular mechanism associated with the formation of tin-doped indium oxide (ITO) nanocrystals. We found that the rea...

Journal: :Bioorganic & medicinal chemistry letters 2011
Juan F Marquez Ruiz Kinga Kedziora Brian Keogh Jacqueline Maguire Mary Reilly Henry Windle Dermot P Kelleher John F Gilmer

The design, synthesis and delivery potential of a new type of benzenesulfonamide cyclo-oxygenase-2 (COX-2) inhibitor prodrug is investigated using celecoxib. The approach involves a double prodrug that is activated first by azoreductases and then by cyclization triggering drug release. We studied the intramolecular aminolysis of the acylsulfonamide. The cyclization was surprisingly rapid at phy...

Journal: :The Journal of organic chemistry 2004
Hyuck Keun Oh Jie Eun Park Dae Dong Sung Ikchoon Lee

The aminolysis of aryl N-ethyl thiocarbamates (EtNHC(=O)SC(6)H(4)Z) with benzylamines (XC(6)H(4)CN(2)NH(2)) in acetonitrile at 30.0 degrees C is investigated. The rates are faster than the corresponding values for aryl N-phenyl thiocarbamates (PhNHC(=O)SC(6)H(4)Z), reflecting a stronger push to expel the leaving group by EtNH than the PhNH nonleaving group in a concerted process. The negative r...

Journal: :Journal of the American Chemical Society 2001
P A Jacobi Y Li

Porphobilinogen lactam methyl ester (3a) has been prepared in seven steps, and approximately 20-30% overall yield, beginning with furfurylamine (4a).(24) Hydrolysis of 3a following the literature procedure then gave porphobilinogen (1). A key intermediate in our synthesis of 3a is the 7-oxonorbornene derivative 7a, which was derived from 4a utilizing a tandem Johnson ortho ester Claisen rearran...

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