The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 3-Hydroxy-3-phenylpropanenitrile(SMILESS: N#CCC(O)C1=CC=CC=C1,cas:17190-29-3) is researched.COA of Formula: C5H7Br. The article 《Nucleophilic ring opening of cyclic sulfites – a convenient method for selective functionalization of 1,2-diols》 in relation to this compound, is published in Acta Chemica Scandinavica. Let’s take a look at the latest research on this compound (cas:17190-29-3).
Regioselective nucleophilic ring cleavage of cyclic sulfites I (e.g, R1 = Ph: R2 = H, Me, Ph) with Nu-M+ (e.g., NaN3, sodiodimethylmalonate, Et4N+CN-) afforded R1CHNuCH(OH)R2 in the case of e.g., NaN3, sodiodimethylmalonate, and R1CH(OH)CHNuR2 in the case of Et4N+CN-. Regioselectivity breaks down with Nu- = Cl-.
If you want to learn more about this compound(3-Hydroxy-3-phenylpropanenitrile)Category: pyrazoles-derivatives, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(17190-29-3).
Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics