Literature DB >> 33146538

Stereomutation of Substituted Bullvalenes.

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


  1 in total

1.  Guest-Dependent Isomer Convergence of a Permanently Fluxional Coordination Cage.

Authors:  André P Birvé; Harshal D Patel; Jason R Price; Witold M Bloch; Thomas Fallon
Journal:  Angew Chem Int Ed Engl       Date:  2022-01-14       Impact factor: 16.823

  1 in total

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