A synthetic method for diversification of the P1′ substituent in phosphinic dipeptides as a tool for exploration of the specificity of the S1′ binding pockets of leucine aminopeptidases

2007 ◽  
Vol 15 (9) ◽  
pp. 3187-3200 ◽  
Author(s):  
Stamatia Vassiliou ◽  
Metaxia Xeilari ◽  
Athanasios Yiotakis ◽  
Jolanta Grembecka ◽  
Małgorzata Pawełczak ◽  
...  
2006 ◽  
Vol 82 (6) ◽  
pp. 1426 ◽  
Author(s):  
Larisa Adamian ◽  
Zheng Ouyang ◽  
Yan Yuan Tseng ◽  
Jie Liang

2019 ◽  
Author(s):  
Shiori Date ◽  
Kensei Hamasaki ◽  
Karen Sunagawa ◽  
Hiroki Koyama ◽  
Chikayoshi Sebe ◽  
...  

<div>We report here a catalytic, Markovnikov selective, and scalable synthetic method for the synthesis of saturated sulfur heterocycles, which are found in the structures of pharmaceuticals and natural products, in one step from an alkenyl thioester. Unlike a potentially labile alkenyl thiol, an alkenyl thioester is stable and easy to prepare. The powerful Co catalysis via a cobalt hydride hydrogen atom transfer and radical-polar crossover mechanism enabled simultaneous cyclization and deprotection. The substrate scope was expanded by the extensive optimization of the reaction conditions and tuning of the thioester unit.</div>


2018 ◽  
Vol 16 (1) ◽  
pp. 34-39
Author(s):  
Yao-Wei Li ◽  
Pei-Ming Zhang ◽  
Rui Li ◽  
Yan Bai ◽  
Yu Yu ◽  
...  

CDI combined with CH3SO3H was found to be highly effective for the cyclization of 2-aminothiophenol derivatives with carboxylic acids under MW condition. Fourteen benzothiazole derivatives were synthesized in good yield and their structures were characterized by 1H-NMR, 13CNMR, IR and mass spectrometry. This simple, rapid synthetic method is believed to provide a useful process for the synthesis of 2-substituted benzothiazole compounds.


2020 ◽  
Vol 17 (8) ◽  
pp. 654-660
Author(s):  
Shermineh Sadat Ghalehbandi ◽  
Dadkhoda Ghazanfari ◽  
Sayed Ali Ahmadi ◽  
Enayatollah Sheikhhosseini

Introduction: We developed a simple, fast and new method for the Fries rearrangement of aryl esters. Materials and Methods: 4-Hydroxy pyridinium triflate functionalized silica is a very efficient, reusable and economically available catalyst for the Fries rearrangement in solvent-free condition and under microwave irradiation. Results and Discussion: Also, a notable selectivity was observed in the presence of 4-hydroxy pyridinium triflate functionalized silica. Conclusion: Selectivity, shorter reaction time, high yield, and easy work-up are advantages of this synthetic method.


2004 ◽  
Vol 69 (22) ◽  
pp. 7710-7719 ◽  
Author(s):  
Naoki Kise ◽  
Kengo Ohya ◽  
Kie Arimoto ◽  
Yutaka Yamashita ◽  
Yuuki Hirano ◽  
...  

2001 ◽  
Vol 32 (1) ◽  
pp. 742
Author(s):  
Dong-Kuk Kim ◽  
Seon-Mi Yoon ◽  
Cha-Joo Park ◽  
Song-Ho Byeon ◽  
Jung-Chul Park ◽  
...  
Keyword(s):  

Nanoscale ◽  
2021 ◽  
Author(s):  
Ping Wang ◽  
Aihua Yuan ◽  
Zhitao Wang ◽  
Xiao Ping Shen ◽  
Hantao Chen ◽  
...  

The hierarchical ZnS/NC dodecahedra are successfully constructed via a two-step synthetic method combining a sulfidation process and subsequent carbonization treatment, benefiting from the inherit merits of zeolitic imidazolate frameworks as...


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