Chemistry of bent bonds. XXXVI. Photolysis of substituted derivatives of 2,3-diazabicyclo[3.1.0]hex-2-ene. Simple route to certain bicyclo[1.1.0]butanes

1973 ◽  
Vol 95 (3) ◽  
pp. 980-982 ◽  
Author(s):  
Paul G. Gassman ◽  
William J. Greenlee
ChemInform ◽  
2014 ◽  
Vol 45 (27) ◽  
pp. no-no
Author(s):  
Daniel J. Tate ◽  
Mohamed Abdelbasit ◽  
Colin A. Kilner ◽  
Helena J. Shepherd ◽  
Stuart L. Warriner ◽  
...  
Keyword(s):  

Tetrahedron ◽  
2014 ◽  
Vol 70 (1) ◽  
pp. 67-74 ◽  
Author(s):  
Daniel J. Tate ◽  
Mohamed Abdelbasit ◽  
Colin A. Kilner ◽  
Helena J. Shepherd ◽  
Stuart L. Warriner ◽  
...  
Keyword(s):  

ChemInform ◽  
2001 ◽  
Vol 32 (5) ◽  
pp. no-no
Author(s):  
Cornelia Heyde ◽  
Ines Zug ◽  
Horst Hartmann
Keyword(s):  

Synlett ◽  
2020 ◽  
Vol 31 (18) ◽  
pp. 1813-1816 ◽  
Author(s):  
Tung T. Nguyen ◽  
Nam T. S. Phan ◽  
Hang T. Pham ◽  
Tuan H. Ho ◽  
Duy Q. Do ◽  
...  

AbstractWe report a simple method for coupling of N,N-dialkyl-3-nitroarenes, elemental sulfur, and activated sp3 C–H bonds in 2-methylazaarenes or arylacetic acids to afford derivatives of 2-arylbenzothiazol-5-amines. Only DABCO base was required, and many heterocycles such as imidazoles, oxazoles, quinolines, and thiophenes were compatible with the reaction conditions. Our approach offers a simple route to useful substituted thiazol-5-amines from commercially available nitroarenes.


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