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.Beck, Thorsten M.; Breit, Bernhard researched the compound: (S)-3,3′-Dibromo-1,1′-bi-2-naphthol( cas:119707-74-3 ).Name: (S)-3,3′-Dibromo-1,1′-bi-2-naphthol.They published the article 《Regio- and enantioselective rhodium-catalyzed addition of 1,3-diketones to allenes: Construction of asymmetric tertiary and quaternary all carbon centers》 about this compound( cas:119707-74-3 ) in Angewandte Chemie, International Edition. Keywords: chiral branched allylated diketone synthesis tertiary quaternary carbon center; allene regioselective enantioselective rhodium catalyst phosphoramidite addition diketone allene; crystal structure phenylhexenyl bistrifluoromethyl phenyl propanedione solvent effect; 1,3-diketones; allenes; asymmetric catalysis; rhodium; γ,δ-unsaturated ketones. We’ll tell you more about this compound (cas:119707-74-3).
An unprecedented highly regio- and enantioselective rhodium-catalyzed addition of 1,3-diketones to terminal and 1,1-disubstituted allenes furnishing asym. tertiary and quaternary all-carbon centers is reported. By applying a RhI/phosphoramidite/TFA catalytic system under mild conditions, the desired chiral branched α-allylated 1,3-diketones could be obtained in good to excellent yields, with perfect regioselectivity and in high enantioselectivity. The reaction shows a broad functional-group tolerance on both reaction partners highlighting its synthetic potential.
This literature about this compound(119707-74-3)Name: (S)-3,3′-Dibromo-1,1′-bi-2-naphtholhas given us a lot of inspiration, and I hope that the research on this compound((S)-3,3′-Dibromo-1,1′-bi-2-naphthol) can be further advanced. Maybe we can get more compounds in a similar way.
Reference:
Bromide – Wikipedia,
bromide – Wiktionary