Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||Synthesis and substitution reactions of N-protected 2-(phenylselenonylmethyl) pyrrolidines|
|Citation:||Australian Journal of Chemistry, 1997; 50(3):181-187|
|Abstract:||<jats:p> Alkyl phenyl selenides derived from the benzeneselenenyl chloride induced cyclization of N-protected pent-4-enylamines can be converted in good yield into the corresponding 2-hydroxymethyl- or 2- alkoxymethyl-substituted pyrrolidines by oxidation to the corresponding selenone, followed by reaction with water (or hydroxide) or with the corresponding alcohol. Details of the reactions and possible mechanisms for the substitution are discussed.</jats:p>|
|Appears in Collections:||Chemistry publications|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.