| Literature DB >> 33146538 |
Oussama Yahiaoui1, Harshal D Patel1, Kylie S Chinner1, Lukáš F Pašteka2, Thomas Fallon1.
Abstract
The stereomutation of substituted bullvalenes is an inevitable consequence of the valence isomerism that automerizes this unique fluxional hydrocarbon. The introduction of external stereogenicity in the substituents expands the reaction graphs and leads to a wealth of complex diastereochemical relationships. In this communication, we explore these possibilities and prepare a range of stereochemically rich substituted bullvalenes. This includes a series of disubstituted bullvalenes with two external stereocenters as a platform for fluxional, shape-diverse compound libraries. We also prepare a tethered bisbullvalene with central stereogenicity in the tether as an ensemble of 900 unique isomers that are completely stereomutable.Entities:
Year: 2020 PMID: 33146538 DOI: 10.1021/acs.orglett.0c03470
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005