170501-70-9

Upstream product

• 99685-96-8 fullerene-C₆₀ 
• 100-46-9 benzylamine 
• 53721-41-8 bis(benzylamino)phenylphosphine oxide 
• 170501-78-7 C₆₇H₇N₃ 

Relevant academic research and scientific papers

Facile and exclusive formation of aziridinofullerenes by acid-catalyzed denitrogenation of triazolinofullerenes

Variously substituted [6,6]closed aziridinofullerenes were exclusively obtained from acid-catalyzed denitrogenation of triazolinofullerenes without formation of relevant [5,6]open azafulleroids, which are the major products on noncatalyzed denitrogenation

Cu(OAc)2-promoted reaction of [60]fullerene with primary amines or diamines

The Cu(OAc)2-promoted reaction of C60 with easily available primary amines allows the concise preparation of aziridinofullerenes. Both alkyl and aryl amines are suitable in this reaction. Moreover, the Cu(OAc)2-promoted re

Hypervalent iodine reagent mediated diamination of [60]fullerene with sulfamides or phosphoryl diamides

A hypervalent iodine-promoted intermolecular diamination reactions of C60 with sulfamides or phosphoryl diamides affords two classes of novel C60-fused cyclic sulfamide or phosphoryl diamide derivatives. The reaction between C60 and sulfamides can be effectively controlled to selectively synthesize diamination products or azafulleroids under PhIO/I2 or PhI(OAc)2/I2 conditions, respectively. Moreover, phosphoryl diamides were first used as an amine source in the diamination of alkenes.

Hypervalent iodine reagent mediated reaction of [60]fullerene with amines

The hypervalent iodine reagent mediated reaction of C60 with various readily available amines for the easy preparation of iminofullerenes has been developed. The reaction between C60 and sulfonamides can be effectively controlled to