Enantioselective Lactonization by π-Acid-Catalyzed Allylic Substitution: A Complement to π-Allylmetal Chemistry.
StackPhos
allylic compounds
enantioselectivity
lactones
π-acid catalysis
Journal
Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543
Informations de publication
Date de publication:
04 10 2021
04 10 2021
Historique:
received:
23
06
2021
pubmed:
24
8
2021
medline:
17
11
2021
entrez:
23
8
2021
Statut:
ppublish
Résumé
Asymmetric allylic alkylation (AAA) is a powerful method for the formation of highly useful, non-racemic allylic compounds. Here we present a complementary enantioselective process that generates allylic lactones via π-acid catalysis. More specifically, a catalytic enantioselective dehydrative lactonization of allylic alcohols using a novel Pd
Identifiants
pubmed: 34423520
doi: 10.1002/anie.202108336
doi:
Substances chimiques
Allyl Compounds
0
Lactones
0
Ligands
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
22224-22229Subventions
Organisme : national science foundation
ID : CHE-1900299
Organisme : NIH HHS
ID : S10 OD021758-01A1
Pays : United States
Organisme : NIH HHS
ID : S10 OD021758-01A1
Pays : United States
Informations de copyright
© 2021 Wiley-VCH GmbH.
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