Simple exploration of 2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid

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 166591-85-1

Synthetic Route of 166591-85-1, 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.166591-85-1, Name is 2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid, molecular formula is C15H19NO4. In a article£¬once mentioned of 166591-85-1

2-TRIFLUOROMETHYL AND 2-PERFLUORO-tert-BUTYLTETRAHYDROFURANS AND ANALOGS OF PYRIMIDINE NUCLEOSIDES BASED ON THEM

2-Trifluoromethyl- and 2-perfluoro-tert-butyltetrahydrofurans and their 5-chlorine-substituted derivatives were synthesized.The latter we used for the production of the analogs of pyrimidine nucleosides, i.e., 1-(5-perfluoroalkyl-2-tetrahydrofuryl)uracils, 5-fluorouracil, and thymine.

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 166591-85-1

Reference£º
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem