Liu, Yue-Jin published the artcileNi(II)/BINOL-catalyzed alkenylation of unactivated C(sp3)-H bonds, Product Details of C22H18O2, the publication is Chemical Communications (Cambridge, United Kingdom) (2015), 51(37), 7899-7902, database is CAplus and MEDLINE.
The first nickel-catalyzed alkenylation of unactivated C(sp3)-H bonds with vinyl iodides is described. The catalytic system comprises an inexpensive and air-stable Ni(acac)2 as the catalyst and BINOL as the ligand, which is highly efficient for the alkenylation of β-Me C(sp3)-H bonds of a broad range of aliphatic carboxamides. The resulting olefins can serve as versatile handles for further preparation Addnl., we also demonstrated the synthesis of functionalized carboxamides bearing α-quaternary carbon centers from simple pivalamide via nickel-catalyzed sequential C(sp3)-H bond functionalization.
Chemical Communications (Cambridge, United Kingdom) published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Product Details of C22H18O2.
Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem