Safety of 3,4-Dimethoxybenzaldehyde. In 2021.0 NEW J CHEM published article about ENANTIOSELECTIVE CONSTRUCTION; STEREOCENTERS; CYCLOPROPANATION; DEAROMATIZATION; STRYCHNINE; ALKALOIDS in [Devi, Manju; Jadhav, Amol P.; Singh, Ravi P.] Indian Inst Technol, Dept Chem, Hauz Khas, New Delhi 110016, India in 2021.0, Cited 47.0. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9.
The stereoselective synthesis of 3,3 ‘-disubstituted oxindoles having all-carbon quaternary stereocenters has been achieved using KOH as a base with an excellent diastereomeric ratio (98 : 2). The practicability of the present methodology has been validated with the synthesis of a series of substrates in good to excellent yields. The aesthetic simplicity, accessibility, and eco-friendly base (KOH) have prompted the broader application of the present methodology in organic synthesis.
About 3,4-Dimethoxybenzaldehyde, If you have any questions, you can contact Devi, M; Jadhav, AP; Singh, RP or concate me.. Safety of 3,4-Dimethoxybenzaldehyde
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