Discovery of 2,3,4-Trihydroxybenzaldehyde

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield. If you are hungry for even more, make sure to check my other article about 2144-08-3, Recommanded Product: 2,3,4-Trihydroxybenzaldehyde.

New Advances in Chemical Research in 2021, Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media. 2144-08-3, Name is 2,3,4-Trihydroxybenzaldehyde, molecular formula is C7H6O4, belongs to isothiazole compound. In a document, author is Li, Ling, introduce the new discover, Recommanded Product: 2,3,4-Trihydroxybenzaldehyde.

An efficient synthesis of bisisothiazole-4-yl disulfides via the demethoxylative thioannulation of alkynyl oxime ethers with odorless elemental sulfur has been first developed. This transformation involves the N-O bond cleavage, the formation of multiple C-S and N-S bonds, providing an efficient way for constructions of both isothiazoles and disulfides. Straightforward elaboration of the products to isothiazole thioethers expands the synthetic utility of this reaction.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield. If you are hungry for even more, make sure to check my other article about 2144-08-3, Recommanded Product: 2,3,4-Trihydroxybenzaldehyde.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com