Synthetic Route of 87392-07-2, 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.87392-07-2, Name is (S)-Tetrahydrofuran-2-carboxylic acid, molecular formula is C5H8O3. In a article£¬once mentioned of 87392-07-2
Compounds of the formula: STR1 wherein R1 is hydrogen, methoxy or formamido; R2 is an acyl group, in particular that of an antibacterially active cephalosporin; CO2 R3 is a carboxy group or a carboxylate anion, or R3 is a readily removable carboxy promoting group or a pharmaceutically acceptable salt-forming group or in vivo hydrolysable ester group; R4 represents hydrogen or up to four substituents, which my be present on any of the carbon atoms in the ring system shown, selected from alkyl, alkenyl, alkynyl, alkoxy, hydroxy, halogen, amino, alkylamino, acylamino, dialkylamino, CO2 R, CONR2, SO2 NR2 where R is hydrogen or alkyl, aryl and heterocyclyl, which may be the same or different and wherein any R4 aryl substituent is optionally substituted by one or more substituents selected from the list from which R4 is selected Y is O, S, SO or SO2 ; n is 0 or 1; and m is 1 or 2; for use in the treatment of bacterial infections in humans and animals.
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 87392-07-2
Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem