Logsdon, DL; Li, YJ; Sobreira, TJP; Ferreira, CR; Thompson, DH; Cooks, RG in [Logsdon, David L.; Li, Yangjie; Thompson, David H.; Cooks, R. Graham] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA; [Sobreira, Tiago Jose Paschoal; Ferreira, Christina R.; Thompson, David H.; Cooks, R. Graham] Purdue Univ, Bindley Biosci Ctr, W Lafayette, IN 47907 USA published High-Throughput Screening of Reductive Amination Reactions Using Desorption Electrospray Ionization Mass Spectrometry in 2020.0, Cited 18.0. Formula: C7H6O2. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.
This study describes the latest generation of a high-throughput screening system that is capable of screening thousands of organic reactions in a single day. This system combines a liquid handling robot with desorption electrospray ionization (DESI) mass spectrometry (MS) for a rapid reaction mixture preparation, accelerated synthesis, and automated MS analysis. A total of 3840 unique reductive amination reactions were screened to demonstrate the throughputs that are capable with the system. Products, byproducts, and intermediates were all monitored in full-scan mass spectra, generating a complete view of the reaction progress. Tandem mass spectrometry experiments were conducted to verify the identity of the products formed. The amine and electrophile reactivity trends represented in the data match what is expected from theory, indicating that the system accurately models the reaction performance. The DESI results correlated well with those generated using more traditional mass spectrometry techniques like liquid chromatography-mass spectrometry, validating the data generated by the system.
About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Logsdon, DL; Li, YJ; Sobreira, TJP; Ferreira, CR; Thompson, DH; Cooks, RG or concate me.. Formula: C7H6O2
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