Formation of Complex α-Imino Esters via Multihetero-Cope Rearrangement of α-Keto Ester Derived Nitrones.
esters
imines
ketones
oxygenations
rearrangement
Journal
Synthesis
ISSN: 0039-7881
Titre abrégé: Synthesis (Stuttg)
Pays: Germany
ID NLM: 7508319
Informations de publication
Date de publication:
Jan 2019
Jan 2019
Historique:
entrez:
5
1
2019
pubmed:
5
1
2019
medline:
5
1
2019
Statut:
ppublish
Résumé
A sequential benzoylation and multihetero-Cope rearrangement of α-keto ester derived nitrones has been developed. The reaction furnishes a diverse array of complex α-imino ester derivatives. The products can be transformed into amino alcohols via LiAlH
Identifiants
pubmed: 30607036
doi: 10.1055/s-0037-1610391
pmc: PMC6311990
mid: NIHMS1001663
doi:
Types de publication
Journal Article
Langues
eng
Pagination
203-212Subventions
Organisme : NIGMS NIH HHS
ID : R35 GM118055
Pays : United States
Références
Org Lett. 2005 Dec 8;7(25):5729-32
pubmed: 16321033
J Org Chem. 2009 Nov 6;74(21):8381-3
pubmed: 19791735
J Am Chem Soc. 2010 Mar 31;132(12):4036-7
pubmed: 20199025
Org Lett. 2011 May 6;13(9):2426-9
pubmed: 21486076
Chem Commun (Camb). 2012 Aug 7;48(61):7568-70
pubmed: 22733086
Chem Rev. 2014 May 28;114(10):5426-76
pubmed: 24628517
Org Lett. 2017 Apr 21;19(8):2126-2129
pubmed: 28397500
Org Lett. 2018 Jul 6;20(13):4048-4051
pubmed: 29906124
Trends Biochem Sci. 1993 Aug;18(8):297-300
pubmed: 8236444