HPLC of Formula: 415918-91-1. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (11bR)-N,N-Bis[(1R)-1-phenylethyl]dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-amine, is researched, Molecular C36H30NO2P, CAS is 415918-91-1, about Synthesis of optically active allylamines by Ir catalyst. Author is Umeda, Rui; Nishiyama, Yutaka.
A review on synthesis of optically active branched allylamines by regioselective and enantioselective allylic amination of allyl carbonates with amines, especially, aromatic amines, in the presence of [Ir(cod)Cl]2 (cod = 1,5-cyclooctadiene) and chiral phosphoramidite (I), synthesis of optically active primary allylamines from allyl carbonates and excess NH3 in the presence of (II), and anal. of the reaction mechanism via Ir-π-allyl complex intermediates.
In addition to the literature in the link below, there is a lot of literature about this compound((11bR)-N,N-Bis[(1R)-1-phenylethyl]dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-amine)HPLC of Formula: 415918-91-1, illustrating the importance and wide applicability of this compound(415918-91-1).
Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics