Abstract
AbstractThe intramolecular hydroamination of carbon‐carbon π‐bonds is an effective method for the rapid construction of nitrogen heterocycles. The rapid evaluation of suitable ligands using virtual screening will aid in the development of a stereoselective analogue of the reaction by predicting effective substrate/ligand combinations. Electronic structure calculations of the relevant transition structures for different nucleophiles and alkynes at the B3LYP/LACVP* level of theory are presented. They provide the basis for the development of a transition state force field by the Q2MM method, which is discussed in detail. The parameter development and performance for the transition state force field is presented.
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