Discovery of 105-13-5

HPLC of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Balaji, S; Balamurugan, G; Ramesh, R; Semeril, D or concate me.

In 2021 ORGANOMETALLICS published article about AEROBIC OXIDATIVE SYNTHESIS; CASCADE SYNTHESIS; QUINAZOLINONES; LIGANDS; FUNCTIONALIZATION; AMINOBENZAMIDES; BENZIMIDAZOLES; HYDROPEROXIDE; HETEROCYCLES; CHEMISTRY in [Balaji, Sundarraman; Balamurugan, Gunasekaran; Ramesh, Rengan] Bharathidasan Univ, Ctr Organometall Chem, Sch Chem, Tiruchirappalli 620024, Tamil Nadu, India; [Semeril, David] Univ Strasbourg, Inst Chim, Lab Chim Inorgan & Catalyse, UMR 7177,CNRS, F-67070 Strasbourg, France in 2021, Cited 78. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. HPLC of Formula: C8H10O2

A convenient protocol for the one-pot synthesis of quinazolin-4(3H)-ones using palladium(II) complexes via dehydrogenative coupling of readily available benzyl alcohols and 2-aminobenzamide has been described. New structurally related Pd(II) N boolean AND O chelating complexes of general configuration [Pd(L)Cl(PPh3)] (where L = dimethylamino benzoylhydrazone ligands) have been designed and synthesized. The formation of the complexes has been recognized by analytical and spectral methods (FT-IR, NMR, HR-MS). The presence of a square-planar geometry around the palladium(II) ion was confirmed by single crystal X-ray diffraction study. A wide range of substituted quinazolinones have been successfully achieved from a diverse range of benzyl alcohols in good to excellent yields using 1.0 mol % of catalyst loading under aerobic conditions. Furthermore, control experiments reveal that the dehydrogenative coupling reaction involves initially the formation of an aldehyde intermediate and subsequent formation of a cyclic aminal intermediate.

HPLC of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Balaji, S; Balamurugan, G; Ramesh, R; Semeril, D or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts