Agasti, Soumitra published the artcileTraceless directing group mediated branched selective alkenylation of unbiased arenes, Related Products of catalysis-chemistry, the publication is Chemical Communications (Cambridge, United Kingdom) (2016), 52(82), 12191-12194, database is CAplus and MEDLINE.
Synthesis of branched olefinated products RR1C=CHR2 [R = C6H5, 2-H3CC6H4, 2,4,6-(CH3)3C6H2, etc.; R1 = 4-ClC6H4, naphthalen-1-yl, 2H-1,3-benzodioxol-5-yl, etc.; R2 = H, CN, C6H5], catalyzed via palladium, facilitated by a C-H activation has been reported. This involves selective insertion of olefins R1CH=C(R2)C(O)OH and subsequent decarboxylation using a completely unbiased benzene ring as the starting precursor. The significance of the protocol has been further highlighted by exhibition of functionality tolerance along with a late-stage modification of the branched olefinated products leading to the formation of other functionalized mols.
Chemical Communications (Cambridge, United Kingdom) published new progress about 1772-76-5. 1772-76-5 belongs to catalysis-chemistry, auxiliary class Benzenes, name is (E)-3-(3-Nitrophenyl)acrylic acid, and the molecular formula is C9H7NO4, Related Products of catalysis-chemistry.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia