An article i-Pr2NMgCl center dot LiCl Enables the Synthesis of Ketones by Direct Addition of Grignard Reagents to Carboxylate Anions WOS:000489200100047 published article about ONE-STEP SYNTHESIS; ONE-POT SYNTHESIS; N-C CLEAVAGE; ORGANOMETALLIC REAGENTS; EFFICIENT SYNTHESIS; CATALYZED SYNTHESIS; DIRECT CONVERSION; ACID-DERIVATIVES; CARBON-MONOXIDE; ACYL CHLORIDES in [Colas, Kilian; dos Santos, A. Catarina V. D.; Mendoza, Abraham] Stockholm Univ, Dept Organ Chem, Arrhenius Lab, S-10691 Stockholm, Sweden in 2019, Cited 82. Recommanded Product: 99-04-7. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7
The direct preparation of ketones from carboxylate anions is greatly limited by the required use of organolithium reagents or activated acyl sources that need to be independently prepared. Herein, a specific magnesium amide additive is used to activate and control the addition of more tolerant Grignard reagents to carboxylate anions. This strategy enables the modular synthesis of ketones from CO2 and the preparation of isotopically labeled pharmaceutical building blocks in a single operation.
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Reference:
Isothiazole – Wikipedia,
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