File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Ir(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents

TitleIr(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents
Authors
Issue Date2018
Citation
Chemical Science, 2018, v. 9, n. 48, p. 8951-8956 How to Cite?
AbstractTransition-metal-catalyzed C-H alkylation reactions directed by aldehydes or ketones have been largely restricted to electronically activated alkenes. Herein, we report a general protocol for the Ir(iii)-catalyzed ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents as the coupling partner. Featuring aniline as an inexpensive catalytic ligand, the method was compatible with a wide variety of benzaldehydes, heterocyclic aldehydes, potassium alkyltrifluoroborates as well as a few α,β-unsaturated aldehydes. An X-ray crystal structure of a benzaldehyde ortho C-H iridation intermediate was also successfully obtained.
Persistent Identifierhttp://hdl.handle.net/10722/327708
ISSN
2023 Impact Factor: 7.6
2023 SCImago Journal Rankings: 2.333
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChen, Xiao Yang-
dc.contributor.authorSorensen, Erik J.-
dc.date.accessioned2023-04-24T05:09:24Z-
dc.date.available2023-04-24T05:09:24Z-
dc.date.issued2018-
dc.identifier.citationChemical Science, 2018, v. 9, n. 48, p. 8951-8956-
dc.identifier.issn2041-6520-
dc.identifier.urihttp://hdl.handle.net/10722/327708-
dc.description.abstractTransition-metal-catalyzed C-H alkylation reactions directed by aldehydes or ketones have been largely restricted to electronically activated alkenes. Herein, we report a general protocol for the Ir(iii)-catalyzed ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents as the coupling partner. Featuring aniline as an inexpensive catalytic ligand, the method was compatible with a wide variety of benzaldehydes, heterocyclic aldehydes, potassium alkyltrifluoroborates as well as a few α,β-unsaturated aldehydes. An X-ray crystal structure of a benzaldehyde ortho C-H iridation intermediate was also successfully obtained.-
dc.languageeng-
dc.relation.ispartofChemical Science-
dc.titleIr(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/c8sc03606c-
dc.identifier.scopuseid_2-s2.0-85058491387-
dc.identifier.volume9-
dc.identifier.issue48-
dc.identifier.spage8951-
dc.identifier.epage8956-
dc.identifier.eissn2041-6539-
dc.identifier.isiWOS:000453011400007-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats