Understanding the Unusual Regioselectivity in the Nucleophilic Ring-Opening Reactions ofgem-Disubstituted Cyclic Sulfates. Experimental and Theoretical Studies

2003 ◽  
Vol 68 (11) ◽  
pp. 4506-4513 ◽  
Author(s):  
Alberto Avenoza ◽  
Jesús H. Busto ◽  
Francisco Corzana ◽  
José I. García ◽  
Jesús M. Peregrina
Molecules ◽  
2021 ◽  
Vol 26 (20) ◽  
pp. 6135
Author(s):  
Valentina Verdoliva ◽  
Giuseppe Digilio ◽  
Michele Saviano ◽  
Stefania De Luca

Aziridine derivatives involved in nucleophilic ring-opening reactions have attracted great interest, since they allow the preparation of biologically active molecules. A chemoselective and mild procedure to convert a peptide cysteine residue into lanthionine via S-alkylation on aziridine substrates is presented in this paper. The procedure relies on a post-synthetic protocol promoted by molecular sieves to prepare lanthionine-containing peptides and is assisted by microwave irradiation. In addition, it represents a valuable alternative to the stepwise approach, in which the lanthionine precursor is incorporated into peptides as a building block.


2018 ◽  
Vol 22 (2) ◽  
pp. 447-501 ◽  
Author(s):  
Rabia Akhtar ◽  
Syed Ali Raza Naqvi ◽  
Ameer Fawad Zahoor ◽  
Sameera Saleem

2019 ◽  
Vol 9 (22) ◽  
pp. 6532-6532
Author(s):  
Shengxin Chen ◽  
Guixiang Zeng ◽  
Yingwei Li ◽  
Bin He ◽  
Ruixia Liu ◽  
...  

Correction for ‘Epoxide ring-opening reaction promoted by ionic liquid reactivity: interplay of experimental and theoretical studies’ by Shengxin Chen et al., Catal. Sci. Technol., 2019, DOI: 10.1039/c9cy00953a.


ChemInform ◽  
2006 ◽  
Vol 37 (40) ◽  
Author(s):  
Jose Sepulveda-Arques ◽  
M. Eugenia Gonzalez-Rosende

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