The use of 7-oxa/azanorbornadienes as synthetic intermediates for the preparation of 3/4-substituted (β-substituted) furans/pyrroles is presented. The method lies in the inverse electron demand Diels-Alder (iEDDA) cycloaddition between a substituted heteronorbornadiene and an electron-poor tetrazine followed by spontaneous fragmentation of the resulting cycloadduct two retro-Diels-Alder (rDA) reactions affording a β-substituted furan/pyrrole. The scope of this tandem iEDDA/rDA/rDA reaction was explored in the preparation of 29 heterocycles. A one-pot procedure starting directly from the alkyne precursors of the heteronorbornadiene intermediates is also described.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507663PMC
http://dx.doi.org/10.1021/acs.joc.3c01145DOI Listing

Publication Analysis

Top Keywords

transferring substituents
4
substituents alkynes
4
alkynes furans
4
furans pyrroles
4
pyrroles heteronorbornadienes
4
heteronorbornadienes intermediates
4
intermediates synthesis
4
synthesis β-substituted
4
β-substituted pyrroles/furans
4
pyrroles/furans 7-oxa/azanorbornadienes
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!