Why do aromatic interactions matter of compound: 707-61-9

In some applications, this compound(707-61-9)Application In Synthesis of 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide, is researched, Molecular C11H13OP, CAS is 707-61-9, about Synthesis of 9H-Pyrrolo[1,2-a]indole and 3H-Pyrrolizine Derivatives via a Phosphine-Catalyzed Umpolung Addition/Intramolecular Wittig Reaction, the main research direction is pyrrolo indole preparation; pyrrolizine preparation; phosphine catalyzed umpolung addition Wittig indole carbaldehyde acetylene dicarboylate.Application In Synthesis of 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide.

The first umpolung addition/intramol. Wittig reaction, catalytic in phosphine, is described. The in situ phosphine oxide reduction was accomplished by the use of silane and a catalytic amount of bis(4-nitrophenyl)phosphate. This catalytic protocol is applicable to the synthesis of a wide range of functionalized 9H-pyrrolo[1,2-a]indoles and pyrrolizines (18 examples, 70-98% yields).

In some applications, this compound(707-61-9)Application In Synthesis of 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide 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