isothiazolium salts
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ARKIVOC ◽  
2010 ◽  
Vol 2011 (6) ◽  
pp. 199-209
Author(s):  
Antje Noack ◽  
Janine Wolf ◽  
Bärbel Schulze
Keyword(s):  

ChemInform ◽  
2010 ◽  
Vol 22 (7) ◽  
pp. no-no
Author(s):  
R. C. DAVIS ◽  
T. J. GRINTER ◽  
D. LEAVER ◽  
R. M. O'NEIL ◽  
G. A. THOMSON
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ChemInform ◽  
2010 ◽  
Vol 26 (34) ◽  
pp. no-no
Author(s):  
B. SCHULZE ◽  
U. OBST ◽  
G. ZAHN ◽  
B. FRIEDRICH ◽  
R. CIMIRAGLIA ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 27 (17) ◽  
pp. no-no
Author(s):  
B. SCHULZE ◽  
S. KIRRBACH ◽  
K. ILLGEN ◽  
P. FUHRMANN
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ChemInform ◽  
2010 ◽  
Vol 27 (45) ◽  
pp. no-no
Author(s):  
B. SCHULZE ◽  
B. FRIEDRICH ◽  
S. WAGNER ◽  
P. FUHRMANN
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ChemInform ◽  
2010 ◽  
Vol 30 (44) ◽  
pp. no-no
Author(s):  
Christine Hartung ◽  
Katrin Illgen ◽  
Joachim Sieler ◽  
Bernd Schneider ◽  
Baerbel Schulze
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2009 ◽  
Vol 64 (6) ◽  
pp. 669-675
Author(s):  
Alexander Eilfeld ◽  
Jens Hunger ◽  
Joachim Sieler ◽  
Barbel Schulze

Stable 3-oxosultams were synthesized by oxidation of the 2-hetaryl-substituted isothiazolium salts. X-Ray crystal structure analyses of the sultams reveal the existence of strong and weak hydrogen bonds, which lead to different interaction combinations and solid state structures. While the bond lengths and angles in the isothiazol rings of the sultams are similar, the dihedral angles between the isothiazol rings and the hetaryl substituents are influenced by the position of the nitrogen atom in the pyridine ring and its substituents. The sultams form chain structures, dimeric head-to-tail structures or two-dimensional networks.


ChemInform ◽  
2008 ◽  
Vol 39 (30) ◽  
Author(s):  
Janine Wolf ◽  
Joachim Sieler ◽  
Baerbel Schulze
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