Pd-Catalyzed Enantioselective (3+2)-Cycloaddition of Vinyl-Substituted Oxyallyl Carbonates with Isocyanates and Ketones

The vinyl-substituted oxyallyl carbonates were exploited as a new C,O-dipole for enantioselective Pd-catalyzed (3+2) cycloaddition. The corresponding oxyallyl-Pd species was weakly nucleophilic to react with activated carbonyl compounds, affording multisubstituted and enantioenriched oxazolidinones and 1,3-dioxolanes with a high degree of chemo- and stereoselectivity. The synthetic transformations of oxazolidinone product were carried out to build enantioenriched α-chiral aminoketone and epoxy derivatives.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:24

Enthalten in:

Organic letters - 24(2022), 11 vom: 25. März, Seite 2099-2103

Sprache:

Englisch

Beteiligte Personen:

Pan, Xuemei [VerfasserIn]
Yu, Limei [VerfasserIn]
Wang, Simin [VerfasserIn]
Wu, Rui [VerfasserIn]
Ou, Chunyan [VerfasserIn]
Xu, Minghui [VerfasserIn]
Chen, Bin [VerfasserIn]
Gao, Yuanji [VerfasserIn]
Ni, Hai-Liang [VerfasserIn]
Hu, Ping [VerfasserIn]
Wang, Bi-Qin [VerfasserIn]
Cao, Peng [VerfasserIn]

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Volltext

Themen:

Journal Article

Anmerkungen:

Date Revised 25.03.2022

published: Print-Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.1021/acs.orglett.2c00290

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM338198962