Research on new synthetic routes about 1265884-98-7

As far as I know, this compound(1265884-98-7)Synthetic Route of C34H22NO2P can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.He, Zhi-Tao; Zhao, Yi-Shuang; Tian, Ping; Wang, Chuan-Chuan; Dong, Han-Qing; Lin, Guo-Qiang researched the compound: 5-(11bR)-Dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-yl-5H-dibenz[b,f]azepine( cas:1265884-98-7 ).Synthetic Route of C34H22NO2P.They published the article 《Copper-Catalyzed Asymmetric Hydroboration of α-Dehydroamino Acid Derivatives: Facile Synthesis of Chiral β-Hydroxy-α-amino Acids》 about this compound( cas:1265884-98-7 ) in Organic Letters. Keywords: dehydroamino acid preparation asym hydroboration copper catalyst; hydroxy amino acid asym preparation. We’ll tell you more about this compound (cas:1265884-98-7).

The Cu-catalyzed asym. conjugate hydroboration reaction of β-substituted α-dehydroamino acid derivatives has been established, affording enantio-enriched syn- and anti-β-boronate-α-amino acid derivatives with excellent combined yields (83-99%, dr ≈ 1:1) and excellent enantioselectivities (92-98% ee). The hydroboration products were expediently converted into valuable β-hydroxy-α-amino acid derivatives, which were widely used in the preparation of chiral drugs and bioactive mols.

As far as I know, this compound(1265884-98-7)Synthetic Route of C34H22NO2P can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

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