Ontology highlight
ABSTRACT:
SUBMITTER: Walton JC
PROVIDER: S-EPMC6217609 | biostudies-literature | 2018 Oct
REPOSITORIES: biostudies-literature
ACS omega 20181016 10
Carbocations are pervasive in contemporary organic synthesis, so new and innocuous methods of making them are always desirable. A theoretical approach revealed that compounds in which radical generation takes place may release carbocations advantageously. The radical types and molecular substructures that promote this effect were identified. The best substructures were found to be 1,3-dicarbonyl compounds, particularly those based on the Meldrum's acid theme. Sulfate esters and dithiane rings co ...[more]