Safety of Methyl 2-methyl-1H-pyrrole-3-carboxylateOn November 30, 2019 ,《N-Alkynyl Pyrrole Based Total Synthesis of Shensongine A》 appeared in Synthesis. The author of the article were Reinus, Brandon J.; Kerwin, Sean M.. The article conveys some information:
A copper-catalyzed N-alkynylation of pyrrole and a gold-catalyzed spiroketalization were key steps in the total synthesis of the pyrrole spiroketal alkaloid shensongine A (I). The preparation of this alkaloid is concise and amenable to the rapid synthesis of a diverse library of compounds The experimental process involved the reaction of Methyl 2-methyl-1H-pyrrole-3-carboxylate(cas: 3168-85-2Safety of Methyl 2-methyl-1H-pyrrole-3-carboxylate)
Methyl 2-methyl-1H-pyrrole-3-carboxylate(cas: 3168-85-2) belongs to pyrroles. Pyrroles are components of more complex macrocycles, including the porphyrinogens and products derived therefrom, including porphyrins of heme, the chlorins, bacteriochlorins, and chlorophylls. Porphobilinogen, a trisubstituted pyrrole, is the biosynthetic precursor to many natural products such as heme.Safety of Methyl 2-methyl-1H-pyrrole-3-carboxylate
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