Computed Properties of C8H8O2. Authors Campbell, MW; Yuan, MB; Polites, VC; Gutierrez, O; Molander, GA in AMER CHEMICAL SOC published article about in [Campbell, Mark W.; Polites, Viktor C.; Molander, Gary A.] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA; [Yuan, Mingbin; Gutierrez, Osvaldo] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA in 2021, Cited 48. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5
Alkenes, ethers, and alcohols account for a significant percentage of bulk reagents available to the chemistry community. The petrochemical, pharmaceutical, and agrochemical industries each consume gigagrams of these materials as fuels and solvents each year. However, the utilization of such materials as building blocks for the construction of complex small molecules is limited by the necessity of prefunctionalization to achieve chemoselective reactivity. Herein, we report the implementation of efficient, sustainable, diaryl ketone hydrogen-atom transfer (HAT) catalysis to activate native C-H bonds for multicomponent dicarbofunctionalization of alkenes. The ability to forge new carbon-carbon bonds between reagents typically viewed as commodity solvents provides a new, more atom-economic outlook for organic synthesis. Through detailed experimental and computational investigation, the critical effect of hydrogen bonding on the reactivity of this transformation was uncovered.
Computed Properties of C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Campbell, MW; Yuan, MB; Polites, VC; Gutierrez, O; Molander, GA 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