Synthetic Route of 288-14-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.288-14-2, Name is Isoxazole, molecular formula is C3H3NO. In a article£¬once mentioned of 288-14-2
Reactions of 5-formyl-and 5-acyl-3,4-dihydro-2H-pyrans and their annelated analogs with nucleophiles
beta-Carbonyl-substituted dihydropyrans are highly useful heterocyclic compounds showing important application in organic synthesis. The increased susceptibility of the dihydropyran ring to the action of various nucleophiles makes these compounds valuable building blocks for the synthesis of a wide variety of hetero- and carbocyclic compounds. On the other hand, the presence of two non-equivalent electrophilic centers poses the problem of selectivity of reactions involving nucleophiles. This chapter will survey the reactivity of 5-formyl- and 5-acyl-3,4-dihydro-2H-pyrans and their annelated analogues with C-, N- and some other mono- and binucleophiles.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 288-14-2
Reference£º
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem