Application In Synthesis of 3,4-Dimethoxybenzaldehyde. Authors Caleffi, GS; Brum, JDC; Costa, AT; Domingos, JLO; Costa, PRR in AMER CHEMICAL SOC published article about in [Caleffi, Guilherme S.; Brum, Juliana de O. C.; Costa, Angela T.; Costa, Paulo R. R.] Univ Fed Rio de Janeiro, Inst Pesquisas Prod Nat, Lab Quim Bioorgan, BR-21941902 Rio De Janeiro, Brazil; [Brum, Juliana de O. C.] Inst Mil Engn, BR-22290270 Rio De Janeiro, Brazil; [Domingos, Jorge L. O.] Univ Estado Rio de Janeiro, Inst Quim, Dept Quim Organ, BR-20550900 Rio De Janeiro, Brazil in 2021.0, Cited 72.0. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9
3-Arylidenechroman-4-ones and 2-arylidene-1-tetralones are hydrogenated to cis-benzylic alcohols in dr’s and er’s up to 99:1 via a C=C and C=O one-pot reduction in the presence of 2-5 mol % Noyori-Ikariya-type Ru-II chiral complexes and HCO2Na as a hydrogen source under asymmetric transfer hydrogenation-dynamic kinetic resolution (ATH-DKR) conditions. The oxidation of theses substrates resulted in the enantioselective synthesis of the natural homoisoflavanone dihydrobonducellin and its carba-analogues.
Application In Synthesis of 3,4-Dimethoxybenzaldehyde. About 3,4-Dimethoxybenzaldehyde, If you have any questions, you can contact Caleffi, GS; Brum, JDC; Costa, AT; Domingos, JLO; Costa, PRR or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles