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1,3-Dipolar Cycloaddition of Isatin-Derived Azomethine Ylides with 2H‐Azirines: Stereoselective Synthesis of 1,3- Diazaspiro[bicyclo[3.1.0]hexane]oxindoles

  • Metaadatok
Tartalom: http://real.mtak.hu/103473/
Archívum: REAL
Gyűjtemény: Status = Published
Subject = Q Science / természettudomány: QD Chemistry / kémia
Subject = Q Science / természettudomány: QD Chemistry / kémia: QD04 Organic chemistry / szerves kémia
Type = Article
Cím:
1,3-Dipolar Cycloaddition of Isatin-Derived Azomethine Ylides with 2H‐Azirines: Stereoselective Synthesis of 1,3- Diazaspiro[bicyclo[3.1.0]hexane]oxindoles
Létrehozó:
Angyal, Anikó
Demjén, András
Harmat, Veronika
Wölfling, János
Puskás, László G.
Kanizsai, Iván
Kiadó:
American Chemical Society
Dátum:
2019
Téma:
QD Chemistry / kémia
QD04 Organic chemistry / szerves kémia
Tartalmi leírás:
A regio- and diastereoselective 1,3-dipolar cycloaddition of 2H-azirines with azomethine ylides generated in situ from isatins and α-amino acids has been elaborated, affording an unprecedented aziridine-fused spiro[imidazolidine-4,3′-oxindole] framework. This one-pot three-component reaction tolerates a wide range of substrates and enables the construction of highly diverse 1,3-diazaspiro[bicyclo[3.1.0]hexane]oxindoles in isolated yields up to 81% under mild conditions.
Nyelv:
magyar
Típus:
Article
NonPeerReviewed
info:eu-repo/semantics/article
Formátum:
text
Azonosító:
Angyal, Anikó and Demjén, András and Harmat, Veronika and Wölfling, János and Puskás, László G. and Kanizsai, Iván (2019) 1,3-Dipolar Cycloaddition of Isatin-Derived Azomethine Ylides with 2H‐Azirines: Stereoselective Synthesis of 1,3- Diazaspiro[bicyclo[3.1.0]hexane]oxindoles. JOURNAL OF ORGANIC CHEMISTRY, 84 (7). pp. 4273-4281. ISSN 0022-3263
Kapcsolat:
10.1021/acs.joc.9b00242