Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Tetrazoles Huisgen tetrazole rearrangement

The Huisgen tetrazole rearrangement is the transformation of C-substituted tetrazole 1 to the corresponding 2,4-disubstituted 1,3,4-oxadiazole 2 by the reaction of carboxylic acid chloride in the presence of a base such as pyridine,... [Pg.309]

Professor Rolf Huisgen discovered the titled reaction in 1958 at the University of Munich. " Huigen s great intuition drove him to ask his Ph.D. student Jurgen Sauer to repeat failed reactions of 5-phenyltetrazole with aroyl chlorides in pyridine that has been run by an an inept postdoctoral fellow, and hence led to the discovery of the named reaction. Since its discovery, the Huisgen tetrazole rearrangement reaction has been used for the synthesis of... [Pg.309]

See other pages where Tetrazoles Huisgen tetrazole rearrangement is mentioned: [Pg.173]    [Pg.706]    [Pg.383]    [Pg.259]    [Pg.309]    [Pg.309]    [Pg.312]    [Pg.696]    [Pg.727]    [Pg.817]    [Pg.685]    [Pg.126]    [Pg.212]    [Pg.313]    [Pg.379]   
See also in sourсe #XX -- [ Pg.309 , Pg.310 , Pg.311 , Pg.312 , Pg.313 , Pg.314 , Pg.315 ]



SEARCH



HUISGEN Tetrazole Rearrangement

HUISGEN Tetrazole Rearrangement

Huisgen

Huisgen rearrangement

Tetrazoles rearrangement

© 2024 chempedia.info