Properties and Exciting Facts About 1265884-98-7

There is still a lot of research devoted to this compound(SMILES：N1(P2OC3=CC=C4C=CC=CC4=C3C5=C6C=CC=CC6=CC=C5O2)C7=CC=CC=C7C=CC8=CC=CC=C81)Recommanded Product: 1265884-98-7, and with the development of science, more effects of this compound(1265884-98-7) can be discovered.

Recommanded Product: 1265884-98-7. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 5-(11bR)-Dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-yl-5H-dibenz[b,f]azepine, is researched, Molecular C34H22NO2P, CAS is 1265884-98-7, about Iridium-Catalyzed Enantioselective Allyl-Allyl Cross-Coupling of Racemic Allylic Alcohols with Allylboronates. Author is Zheng, Yu; Yue, Bei-Bei; Wei, Kun; Yang, Yu-Rong.

Carreira’s iridium-(P, olefin) phosphoramidite-based catalytic system that allows asym. allyl-allylboronate cross-coupling with high enantioselectivity is reported. This transformation tolerates a large variety of racemic branched allylic alcs. and allylboronate substrates. The utility of the coupling is demonstrated in a concise catalytic asym. synthesis of (-)-preclamol (I).

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Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem