Introduction of a new synthetic route about 119707-74-3

Different reactions of this compound((S)-3,3′-Dibromo-1,1′-bi-2-naphthol)Quality Control of (S)-3,3′-Dibromo-1,1′-bi-2-naphthol require different conditions, so the reaction conditions are very important.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: (S)-3,3′-Dibromo-1,1′-bi-2-naphthol, is researched, Molecular C20H12Br2O2, CAS is 119707-74-3, about Enantioselective conjugate allylation of cyclic enones, the main research direction is cycloketone enantioselective synthesis; cyclic enone allylation dibromobinaphthol catalyst Cope rearrangement KH.Quality Control of (S)-3,3′-Dibromo-1,1′-bi-2-naphthol.

Enantioselective organocatalytic 1,2-allylation of a cyclic enone followed by anionic oxy-Cope rearrangement delivered the ketone as a mixture of diastereomers. This appears to be a general method for the net enantioselective conjugate allylation of cyclic enones.

Different reactions of this compound((S)-3,3′-Dibromo-1,1′-bi-2-naphthol)Quality Control of (S)-3,3′-Dibromo-1,1′-bi-2-naphthol require different conditions, so the reaction conditions are very important.

Reference:
Bromide – Wikipedia,
bromide – Wiktionary