Chemoselective Suzuki–Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate

Add time:09/02/2019    Source:sciencedirect.com

Arylated naphthalenes were prepared by Suzuki–Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate. The reactions proceeded with very good chemoselectivity in favor of the triflate group, due to additive electronic ortho electronic effects.

We also recommend Trading Suppliers and Manufacturers of METHYL 3-METHOXY-2-NAPHTHOATE (cas 13041-60-6). Pls Click Website Link as below: cas 13041-60-6 suppliers

Prev:Enhanced nucleophilic substitution with coordinated 4,4‘-dichloro-2,2‘-bipyridine: X-ray structures of 4,4‘-dichloro-2,2‘-bipyridine (Bipy-Cl2), cis-dichlorobis(4,4‘-dichloro-2,2‘-bipyridine)rhodium(III) hexafluorophosphate [Rh](PF6), and tris(4,4‘-dichloro-2,2‘-bipyridine)ruthenium(II) hexafluorophosphate [Ru](PF6)2
Next:Intramolecular hydrogen bonding of methoxynaphthoic acids and methyl hydroxynaphthoates)