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Pregled bibliografske jedinice broj: 374839

Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases


Stipetić, Irena; Roje, Marin; Hameršak, Zdenko
Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases // Synlett, 2008 (2008), 20; 3149-3152 doi:10.1055/s-0028-1087367 (međunarodna recenzija, članak, znanstveni)


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Naslov
Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases

Autori
Stipetić, Irena ; Roje, Marin ; Hameršak, Zdenko

Izvornik
Synlett (0936-5214) 2008 (2008), 20; 3149-3152

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
asymmetric synthesis ; aziridines ; enantioselectivity ; imine ; ylide

Sažetak
Asymmetric synthesis of 2, 3-disubstituted N-Boc, N-SES, and N-Ts aziridines starting from N-protected imines, using sulfonium salt derived from Eliel’ s oxathiane, is reported. Sodium hydride was successfully used as a substitute for the phosphazene base EtP2 without any loss of yield, enantioselectivity, or diastereoselectivity.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
098-0982933-2908 - Kiralni građevni blokovi za biološki aktivne molekule. Sinteza i reaktivnost (Hameršak, Zdenko, MZOS ) ( POIROT)

Ustanove:
Institut "Ruđer Bošković", Zagreb

Profili:

Avatar Url Irena Dokli (autor)

Avatar Url Zdenko Hameršak (autor)

Avatar Url Marin Roje (autor)

Citiraj ovu publikaciju

Stipetić, Irena; Roje, Marin; Hameršak, Zdenko
Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases // Synlett, 2008 (2008), 20; 3149-3152 doi:10.1055/s-0028-1087367 (međunarodna recenzija, članak, znanstveni)
Stipetić, I., Roje, M. & Hameršak, Z. (2008) Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases. Synlett, 2008 (20), 3149-3152 doi:10.1055/s-0028-1087367.
@article{article, year = {2008}, pages = {3149-3152}, DOI = {10.1055/s-0028-1087367}, keywords = {asymmetric synthesis, aziridines, enantioselectivity, imine, ylide}, journal = {Synlett}, doi = {10.1055/s-0028-1087367}, volume = {2008}, number = {20}, issn = {0936-5214}, title = {Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases}, keyword = {asymmetric synthesis, aziridines, enantioselectivity, imine, ylide} }
@article{article, year = {2008}, pages = {3149-3152}, DOI = {10.1055/s-0028-1087367}, keywords = {asymmetric synthesis, aziridines, enantioselectivity, imine, ylide}, journal = {Synlett}, doi = {10.1055/s-0028-1087367}, volume = {2008}, number = {20}, issn = {0936-5214}, title = {Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases}, keyword = {asymmetric synthesis, aziridines, enantioselectivity, imine, ylide} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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