The important role of 1265884-98-7

Although many compounds look similar to this compound(1265884-98-7)Related Products of 1265884-98-7, numerous studies have shown that this compound(SMILES:N1(P2OC3=CC=C4C=CC=CC4=C3C5=C6C=CC=CC6=CC=C5O2)C7=CC=CC=C7C=CC8=CC=CC=C81), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. 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 C3-selective asymmetric allylation of 7-azaindoles with secondary allylic alcohols, the main research direction is azaindole secondary allylic alc iridium catalyst allylation; aryl allyl pyrrolopyridine preparation enantioselective regioselective.Related Products of 1265884-98-7.

Iridium-catalyzed C3-selective asym. allylation of 7-azaindoles with racemic secondary allylic alcs. to give only branched allylation products in good to high yields with high enantioselectivity (up to >99.5% ee) was reported. Allylic alcs. and 7-azaindoles with a variety of functional groups including halogen and heteroaromatic groups were compatible with the reaction conditions. Furthermore, transformations of the obtained allylation products were demonstrated without a significant loss of enantiomeric excess.

Although many compounds look similar to this compound(1265884-98-7)Related Products of 1265884-98-7, numerous studies have shown that this compound(SMILES:N1(P2OC3=CC=C4C=CC=CC4=C3C5=C6C=CC=CC6=CC=C5O2)C7=CC=CC=C7C=CC8=CC=CC=C81), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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