dc.contributor.author
Puig, Jordi
dc.contributor.author
Bonjoch, Josep
dc.contributor.author
Bradshaw, Ben
dc.date.issued
2025-01-16T19:26:47Z
dc.date.issued
2025-01-16T19:26:47Z
dc.date.issued
2023-08-30
dc.date.issued
2025-01-16T19:26:47Z
dc.identifier
https://hdl.handle.net/2445/217580
dc.description.abstract
The use of isocyanides as acceptor groups in metal–hydride hydrogen atom transfer (MHAT) coupling reactions with nonactivated alkenes to form heterocycles is described. Monosubstituted alkenes couple and cyclize directly, whereas more substituted alkenes proceed via a two-step, one-pot procedure involving MHAT reductive cyclization followed by a MHAT Minisci coupling upon the addition of acid. To highlight the utility of the methodology, a diverse variety of substituted heterocycles such as phenanthridines, indoles, and isoquinolines were prepared.
dc.format
application/pdf
dc.format
application/pdf
dc.publisher
American Chemical Society
dc.relation
Reproducció del document publicat a: https://doi.org/10.1021/acs.orglett.3c02358
dc.relation
Organic Letters, 2023, vol. 25, num.35, p. 6539-6543
dc.relation
https://doi.org/10.1021/acs.orglett.3c02358
dc.rights
cc by (c) Jordi Puig, et al., 2023
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.title
Isocyanides as Acceptor Groups in MHAT Reactions with Unactivated Alkenes
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion