Discovery of 288-16-4

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Reference of 288-16-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 288-16-4, in my other articles.

Reference of 288-16-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.288-16-4, Name is Isothiazole, molecular formula is C3H3NS. In a Article in Press£¬once mentioned of 288-16-4

Dithioester-enabled chemodivergent synthesis of acids, amides and isothiazoles via CC bond cleavage and CO/CN/CS bond formations under metal- and catalyst-free conditions

An operationally simple and user-friendly process to access privileged scaffolds such as acids, amides and isothiazoles has been devised employing beta-ketodithioesters for the first time. Remarkably, the new protocol involves combination of C. C bond cleavage and C. O/C. N/N. S bond formations in one-pot. Aqueous ammonia led to the formation of skeletally distinct amide and isothiazole, whereas aqueous NaOH enabled the formation of aromatic acid near quantitative yield. This practical approach, which can dramatically streamline the synthesis of simple molecules, is highly chemoselective, cost-effective, amenable to gram scale, insensitive to moisture as well as bears high functional group compatibility.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Reference of 288-16-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 288-16-4, in my other articles.

Reference£º
Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com