Chemistry of Tetrathiomolybdate:  Aziridine Ring Opening Reactions and Facile Synthesis of Interesting Sulfur Heterocycles

2005 ◽  
Vol 127 (37) ◽  
pp. 12760-12761 ◽  
Author(s):  
Devarajulu Sureshkumar ◽  
Srinivasa Murthy Koutha ◽  
Srinivasan Chandrasekaran
2009 ◽  
pp. 5722 ◽  
Author(s):  
Kazutaka Seki ◽  
Rongmin Yu ◽  
Yumi Yamazaki ◽  
Yasuhiro Yamashita ◽  
Shū Kobayashi

2015 ◽  
Vol 13 (39) ◽  
pp. 10050-10059 ◽  
Author(s):  
T. Cytlak ◽  
M. Saweliew ◽  
M. Kubicki ◽  
H. Koroniak

The synthesis of phosphonated derivatives of trifluoromethyl aziridines by two methods and their application in ring opening reactions have been demonstrated.


2015 ◽  
Vol 56 (38) ◽  
pp. 5269-5271 ◽  
Author(s):  
N. Viswanadh ◽  
R. Velayudham ◽  
S. Jambu ◽  
M. Sasikumar ◽  
M. Muthukrishnan

2007 ◽  
Vol 72 (10) ◽  
pp. 3859-3862 ◽  
Author(s):  
Diego Savoia ◽  
Giuseppe Alvaro ◽  
Romano Di Fabio ◽  
Andrea Gualandi

ChemInform ◽  
2010 ◽  
Vol 41 (9) ◽  
Author(s):  
Devarajulu Sureshkumar ◽  
Venkataraman Ganesh ◽  
Ravindran Sasitha Vidyarini ◽  
Srinivasan Chandrasekaran

1990 ◽  
Vol 43 (6) ◽  
pp. 1123 ◽  
Author(s):  
RD Allan ◽  
HW Tran

Nucleophilic ring opening of the protonated salt of 2-(4-chlorophenyl ) aziridine with substituted thiols provides a very simple route to β- phenylethylamine derivatives which are analogues of the GABAB receptor agonist baclofen and its antagonists phaclofen and saclofen.


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