Synthesis of biindolyls by the reaction of indoles with indolin-2-ones and phosphoryl chloride or trifluoromethanesulfonic anhydride

Tetrahedron ◽  
1996 ◽  
Vol 52 (13) ◽  
pp. 4697-4708 ◽  
Author(s):  
David StC. Black ◽  
Andrew J. Ivory ◽  
Naresh Kumar
SynOpen ◽  
2021 ◽  
Author(s):  
Valerio Zullo ◽  
Antonella Petri ◽  
Anna Iuliano

The synthesis of 6-aminoisomannide is easily achieved starting from the renewable, inexpensive and commercially available isosorbide, in 66% overall yield. A biocatalysed highly regioselective acetylation of the 3-endo hydroxyl group of isosorbide was followed by the stereospecific interconversion of the 6-exo hydroxyl group into azido group, through reaction with trifluoromethanesulfonic anhydride followed by nucleophilic displacement of the triflate group by sodium azide. Finally, reduction of the azido group and deacetylation of the 3-hydroxy group were performed one pot by using LiAlH4.


1982 ◽  
Vol 35 (7) ◽  
pp. 1391 ◽  
Author(s):  
AJ Liepa

N,N-Dialkyl derivatives of 3-aminoisoquinoline have been prepared by reaction of nitriles with various arylacetic acid tertiary amides in the presence of phosphoryl chloride. The synthesis has been extended to include a benzoisoquinoline and annulated isoquinolines by the selection of appropriate amide and nitrile precursors.


2021 ◽  
Author(s):  
Akira Yoshimura ◽  
Christopher Huss ◽  
Akio Saito ◽  
Tsugio Kitamura ◽  
Viktor V Zhdankin

2-Iodosylbenzoic acid in the presence of trifluoromethanesulfonic anhydride is an efficient oxidant and electrophilic reagent useful for preparation of the corresponding alkenyl and aryliodonium salts. Compared to the previously reported...


1993 ◽  
Vol 47 ◽  
pp. 344-357 ◽  
Author(s):  
Frank Birkeneder ◽  
Rolf Willestofte Berg ◽  
Niels Janniksen Bjerrum ◽  
Anna V. Luzikova ◽  
Jon Brunvoll ◽  
...  

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