Reakcje asymetrycznego otwierania pierścienia azyrydyn

Prusinowska, N.

Artykuł - szczegóły

Tytuł artykułu

Reakcje asymetrycznego otwierania pierścienia azyrydyn

Autorzy

Prusinowska N.

Treść / Zawartość

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Warianty tytułu

Asymmetric aziridine ring opening reactions

Języki publikacji

Abstrakty

Aziridines, the nitrogenous analogues of epoxides, are useful building blocks for the synthesis of various functional materials and biologically active compounds. The reactivity of aziridines toward ring opening and expansion is dependent upon their extremely strained ring structures. Among the procedures of ring opening of aziridines, a nucleophilic ring-opening reaction is one of the major routes to highly functionalized compounds (Scheme 2). This short review focused on essentiac asymmetric ring opening reactions of aziridines including enantioselective ring opening of meso-aziridines and kinetic resolution of racemic aziridines with various hetero and carbon nucleophiles towards the synthesis of highly enantiomerically enriched 1,2-difunctionalized fine chemicals.

Słowa kluczowe

azyrydyny desymetryzacja kataliza asymetryczna rozdział kinetyczny reakcje otwierania pierścienia

aziridines desymmetrization asymmetric catalysis kinetic resolution ring opening reaction

Wydawca

Polskie Towarzystwo Chemiczne

Czasopismo

Wiadomości Chemiczne

Rocznik

2013

Tom

[Z] 67, 5-6

Strony

585--618

Opis fizyczny

Bibliogr. 67 poz., schem.

Twórcy

autor

Prusinowska N.

nwascin@amu.edu.pl

Uniwersytet im. Adama Mickiewicza, Wydział Chemii ul. Umultowska 89b , 61-614 Poznań

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Typ dokumentu

Bibliografia

Identyfikator YADDA

bwmeta1.element.baztech-62829553-e336-4415-96a0-2e2c3761a4f4