Enzymology of carbon–sulfur bond formation

2001 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
A Marquet
Keyword(s):  
2021 ◽  
Vol 27 (1) ◽  
pp. 17-23
Author(s):  
Guniganti Balakishan ◽  
Gullapalli Kumaraswamy ◽  
Vykunthapu Narayanarao ◽  
Pagilla Shankaraiah

Abstract A Cu(II)-catalyzed Csp2-Se and Csp2-Sulfur bond formation was achieved with moderate to good yields without the aid of Lewis acid and base. The reaction is compatible with a wide range of heterocycles such as benzothiazole, thiazole, and imidazole. Also, this typical protocol is found to be active in thio-selenation via S-H activation. Additionally, we proposed a plausible mechanistic pathway involving Cu(III) putative intermediate.


2018 ◽  
Vol 47 (18) ◽  
pp. 6333-6343 ◽  
Author(s):  
Lucy Currie ◽  
Luca Rocchigiani ◽  
David L. Hughes ◽  
Manfred Bochmann

Thiols were found to cleave Au–C bonds in (C^N^C)gold(iii) pincer complexes and to induce C–S reductive elimination reactions, to give aryl thioethers.


2020 ◽  
Vol 362 (14) ◽  
pp. 2801-2846 ◽  
Author(s):  
David J. Jones ◽  
Eileen M. O'Leary ◽  
Timothy P. O'Sullivan

ChemInform ◽  
2010 ◽  
Vol 27 (25) ◽  
pp. no-no
Author(s):  
J. E. BALDWIN ◽  
R. M. ADLINGTON ◽  
D. G. MARQUESS ◽  
A. R. PITT ◽  
M. J. PORTER ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document