Extended knowledge of 1265884-98-7

In some applications, this compound(1265884-98-7)Computed Properties of C34H22NO2P is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

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, Research Support, Non-U.S. Gov’t, Angewandte Chemie, International Edition called Asymmetric Total Synthesis of Mycoleptodiscin A, Author is Zhou, Shupeng; Chen, Hao; Luo, Yijie; Zhang, Wenhao; Li, Ang, the main research direction is mycoleptodiscin A asym total synthesis; CN bond formation; allylic substitution; indole terpenoids; iridium catalysis; polyene cyclization.Computed Properties of C34H22NO2P.

The first total synthesis of mycoleptodiscin A, a structurally unusual indolosesquiterpenoid possessing an ortho-benzoquinone motif, has been accomplished. A sulfone alkylation coupled two readily available fragments to give an aryl triene intermediate. The tetracyclic core of the mol. was assembled through a highly enantioselective iridium-catalyzed polyene cyclization. The benzylic homologation was achieved by a cationic cyanation. The indole motif was constructed via a copper-mediated intramol. C-N bond formation at a late stage.

In some applications, this compound(1265884-98-7)Computed Properties of C34H22NO2P is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

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