Can You Really Do Chemisty Experiments About 1265884-98-7

After consulting a lot of data, we found that this compound(1265884-98-7)Electric Literature of C34H22NO2P can be used in many types of reactions. And in most cases, this compound has more advantages.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1265884-98-7, is researched, SMILESS is N1(P2OC3=CC=C4C=CC=CC4=C3C5=C6C=CC=CC6=CC=C5O2)C7=CC=CC=C7C=CC8=CC=CC=C81, Molecular C34H22NO2PJournal, Article, Angewandte Chemie, International Edition called Iridium-Catalyzed Enantioselective Allylic Alkylation with Functionalized Organozinc Bromides, Author is Hamilton, James Y.; Sarlah, David; Carreira, Erick M., the main research direction is carbonate racemic enantioselective regioselective allylic alkylation organozinc iridium catalyst; alkene branched asym synthesis; alkylation; allylic compounds; enantioselectivity; iridium; zinc.Electric Literature of C34H22NO2P.

Iridium-catalyzed enantioselective allylic alkylation of branched racemic carbonates R1CH(OBoc)CH:CH2 (R1 = MeCH:CH, Ph, 3-MeOC6H4, 3-thienyl, 2-naphthyl, PhCH2CH2CC, etc.) with functionalized alkylzinc bromide reagents R2ZnBr [R2 = EtO2C(CH2)3, NC(CH2)4, 1,3-dioxolan-2-ylmethyl, etc.] is described. Enabled by a chiral Ir/(P,olefin) complex, this method allows allylic substitution with various primary and secondary alkyl nucleophiles with excellent regio- and enantioselectivities. The developed reaction was showcased in a concise, asym. synthesis of (-)-preclamol.

After consulting a lot of data, we found that this compound(1265884-98-7)Electric Literature of C34H22NO2P can be used in many types of reactions. And in most cases, this compound has more advantages.

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