1265831-02-4Relevant articles and documents
Preparation and reactions of (1 H-tetrazol-5-yl)zinc pivalates
Tüllmann, Carl Phillip,Steiner, Sebastian,Knochel, Paul
, p. 2357 - 2363 (2020)
The preparation and reactivity of new solid heterocyclic organozinc reagents, namely N -protected (1 H -tetrazol-5-yl)zinc pivalates, as storable solids with appreciably air and moisture stability are reported. They are obtained in high yields from protected 1 H -tetrazoles by de-protonation using the mixed zinc-magnesium base TMPZnCl·Mg(OPiv) 2(abbreviated as TMPZnOPiv; TMP = 2,2,6,6-tetramethylpiperidyl). Subsequent cross-couplings and copper-catalyzed electrophilic aminations using hydroxylamine benzoates give access to functionalized 1 H -tetrazoles while tolerating many functional groups.
Three-component strategy toward 5-membered heterocycles from isocyanide dibromides.
Kaim, Laurent El,Grimaud, Laurence,Patil, Pravin
, p. 1261 - 1263 (2011/04/25)
A three-component strategy starting from isocyanides allows a straightforward synthesis of five-membered ring heterocycles. New cascades were developed involving the addition of a nitrogenated nucleophile-an azide or a tetrazole-on isocyanide dibromides,