Mollica, A.Zengin, Gökhan2020-03-262020-03-2620161573-4072https://dx.doi.org/10.2174/1573407212666160511162638https://hdl.handle.net/20.500.12395/34327Threonine-proline chimeras are not so abundant in nature as the other proine-chimeras and their functionalization is also restricted to the third position on the pyrrolidine ring. Despite these aspects the synthetic procedures adopted to obtain these products are straightforward and well-described in literature, as reported in the following review. © 2016 Bentham Science Publishers.en10.2174/1573407212666160511162638info:eu-repo/semantics/closedAccessDeckmann reactionDiastereoselective cyclizationMichael condensationSharpless epoxidationThreonine-proline chimerasReview123221228Q3