Rush Scaggs, W.; Scaggs, Toya D.; Snaddon, Thomas N. published an article about the compound: Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate( cas:51856-79-2,SMILESS:O=C(OC)CC1=CC=CN1C ).Safety of Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:51856-79-2) through the article.
Herein we describe the direct enantioselective Lewis base/Pd catalyzed α-allylation of pyrrole acetic acid esters. This provides high isolated yields of highly enantioenriched products, e.g., I, and exhibits broad reaction scope with respect to both reaction partners. The products can be readily elaborated in a manner which points towards potential applications in target directed synthesis.
There is still a lot of research devoted to this compound(SMILES：O=C(OC)CC1=CC=CN1C)Safety of Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate, and with the development of science, more effects of this compound(51856-79-2) can be discovered.
Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem