Reference of 569-31-3, 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.569-31-3, Name is 6,7-Dimethoxy-3H-1-isobenzofuranone, molecular formula is C10H10O4. In a article£¬once mentioned of 569-31-3
Synthesis of phthalideisoquinolines by direct coupling of phthalide anions with 3,4-dihydroisoquinolinium salts
The condensation of phthalide anions, derived from phthalide itself and from its 6,7- and 5,6-dimethoxy derivatives, with 6,7-dimethoxy-2-methyl-3,4-dihydroisoquinoline is described.The reaction products obtained in ca. 40percent yield are easily separable mixtures of substituted (+/-)-erythro and (+/-)-threo-phthalidetetrahydroisoquinolines.The reaction is potentially useful for synthesis of naturally occurring alkaloids of this family.
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 569-31-3
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Benzofuran – Wikipedia,
Benzofuran | C8H3144O – PubChem