ChemInform Abstract: A STUDY OF PERISELECTIVITY IN THE THERMAL CYCLIZATION REACTIONS OF DIENE-CONJUGATED DIAZO COMPOUNDS: 1,7-CYCLIZATION AS A ROUTE TO 3H-1,2-DIAZEPINES AND 1,5-CYCLIZATION LEADING TO NEW REARRANGEMENT REACTIONS OF 3H-PYRAZOLES

1985 ◽  
Vol 16 (6) ◽  
Author(s):  
I. R. ROBERTSON ◽  
J. T. SHARP
ChemInform ◽  
1987 ◽  
Vol 18 (34) ◽  
Author(s):  
N. KAWAHARA ◽  
T. SHIMAMORI ◽  
T. ITOH ◽  
H. TAKAYANAGI ◽  
H. OGURA

1987 ◽  
Vol 35 (2) ◽  
pp. 457-467 ◽  
Author(s):  
NORIO KAWAHARA ◽  
TAKAKO SHIMAMORI ◽  
TSUNEO ITOH ◽  
HIROAKI TAKAYANAGI ◽  
HARUO OGURA

1987 ◽  
Vol 52 (1) ◽  
pp. 113-119 ◽  
Author(s):  
Miroslav Veverka ◽  
Miroslav Marchalín

Ethyl (3-substituted 5-thioxo-1,2,4-triazolin-4-yl)acetates were prepared by addition-cyclization reaction of ethyl isothiocyanatoacetate with carboxylic acid hydrazides in the presence of sodium ethoxide. Thermal cyclization of the adduct in dimethylformamide afforded 1-acetamido-2-thiohydantoin. The effect of substituents on the cyclization course and the thione-thiol tautomerism are discussed.


1981 ◽  
Vol 46 (12) ◽  
pp. 3128-3133 ◽  
Author(s):  
Michal Uher ◽  
Dušan Ilavský ◽  
Jozef Foltín ◽  
Katarína Škvareninová

Reactions of carbonyl isothiocyanates with enamines of the type CH3-C(NH2)=CH-X (X = CN, COOC2H5, or COCH3) were investigated. The formation of products of AdN, SN, and cyclization reactions is discussed on the basis of their IR, UV and mass spectra. In one case, the thermal cyclization was followed by differential thermal analysis.


2012 ◽  
Vol 53 (7) ◽  
pp. 738-743 ◽  
Author(s):  
László Lengyel ◽  
Tibor Zs. Nagy ◽  
Gellért Sipos ◽  
Richard Jones ◽  
György Dormán ◽  
...  

2017 ◽  
Vol 53 (49) ◽  
pp. 6577-6580 ◽  
Author(s):  
Katharina J. Hock ◽  
Lucas Mertens ◽  
Renè Hommelsheim ◽  
Robin Spitzner ◽  
Rene M. Koenigs

Safe rearrangement reactions of sulfides with in situ generated diazo compounds have been developed. Transient generation of, for example, diazo acetonitrile followed by iron catalysed Doyle–Kirmse reaction generates valuable building blocks for drug discovery.


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