Anthelmintics

(8aR)-1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrazine:dihydrochloride.

(9aS)-2-benzyl-1,3,4,6,7,8,9,9a-octahydropyrazino[1,2-a]pyrazine.

(9aS)-Octahydropyrazino[2，1-c][1，4]oxazine.

(9aS)-Octahydropyrazino[2，1-c][1，4]oxazine.

(9aS)-Octahydropyrazino[2，1-c][1，4]oxazine.

Application Catalyst for isomerization and anti-Markovnikov arylation of olefins Reactant for: Oxidative addition of perfluoroalkyl iodides Synthesis of iridium heterocycles Scaffolding of iridium complexes Metal carbonyl cluster synthesis

(D-Ala¹¹]bombesin.

Stoichiometric oxidant in the TEMPO oxidation of nerol to neral. Oxidant employed in the rhodium-catalyzed aziridination of olefins with sulfamate esters. Unactivated sp3 C-H bonds of both oxime and pyridine substrates undergo highly regio- and

Stoichiometric oxidant in the TEMPO oxidation of nerol to neral. Oxidant employed in the rhodium-catalyzed aziridination of olefins with sulfamate esters. Unactivated sp3 C-H bonds of both oxime and pyridine substrates undergo highly regio- and

Stoichiometric oxidant in the TEMPO oxidation of nerol to neral. Oxidant employed in the rhodium-catalyzed aziridination of olefins with sulfamate esters. Unactivated sp3 C-H bonds of both oxime and pyridine substrates undergo highly regio- and

Stoichiometric oxidant in the TEMPO oxidation of nerol to neral. Oxidant employed in the rhodium-catalyzed aziridination of olefins with sulfamate esters. Unactivated sp3 C-H bonds of both oxime and pyridine substrates undergo highly regio- and

Stoichiometric oxidant in the TEMPO oxidation of nerol to neral. Oxidant employed in the rhodium-catalyzed aziridination of olefins with sulfamate esters. Unactivated sp3 C-H bonds of both oxime and pyridine substrates undergo highly regio- and