Krascsenicsova, Katarina’s team published research in Chemical Communications (Cambridge, United Kingdom) in | CAS: 126613-06-7

Krascsenicsova, Katarina published the artcileStereoconservative Negishi arylation and alkynylation as an efficient approach to enantiopure 2,2′-diarylated 1,1′-binaphthyls, Product Details of C22H12F6O6S2, the publication is Chemical Communications (Cambridge, United Kingdom) (2004), 2606-2607, database is CAplus and MEDLINE.

Negishi arylation and alkynylation of easily synthesized chiral 2,2′-diiodo-1,1′-binaphthyl rapidly proceeds in refluxing THF under microwave irradiation conditions affording enantiopure 2,2′-R₂-1,1′-binaphthyls (R = Ph, 4-MeC₆H₄, 2-MeOC₆H₄, 2-furyl, 3-pyridyl, Me₃SiCC, PhCC, etc.) in good to excellent yields.

Chemical Communications (Cambridge, United Kingdom) published new progress about 126613-06-7. 126613-06-7 belongs to esters-buliding-blocks, auxiliary class Chiral Diphenols, name is (R)-[1,1′-Binaphthalene]-2,2′-diyl bis(trifluoromethanesulfonate), and the molecular formula is C22H12F6O6S2, Product Details of C22H12F6O6S2.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics