From Chemical Serendipity to Translational Chemistry: New Findings in the Reactivity of Palladacycles

ChemistryOpen. 2018 Aug 12;7(10):754-763. doi: 10.1002/open.201800036. eCollection 2018 Oct.

Abstract

In the world of science, in particular the section concerning the field of chemistry, when the results encountered during the experiment do not meet our expectations, our shrewdness may play an important role to open up new unexplored fields that could be much more interesting than what we were seeking. In those cases, our research undergoes an unforeseen shift, delivering novel and challenging results that may altogether alter our point of view and our future work. We have then struck serendipity. Specifically, in our investigation linked to palladacycles we have found that the new trends in their reactivity, as well as in their structure, have been, in many cases, related to this experience, broadening our research scope within this field. Herein, we describe our most relevant findings, which have shed new light upon the reactivity of palladacycles, thus opening new routes that lead to novel unexpected structures.

Keywords: Schiff base; palladacycles; serendipity; thiosemicarbazone; translational chemistry.

Publication types

  • Review