Highly Efficient Asymmetric Synthesis of Chiral γ‑Alkenyl Butenolides Catalyzed by Chiral N,N′‑Dioxide–Scandium(III) Complexes
The asymmetric synthesis of γ-alkenyl butenolides was accomplished by conjugated addition of butenolides to alkynones. Both terminal alkynones and nonterminal alkynones were applicable to the N,N′-dioxide–scandium(III) catalytic system. The corresponding products were obtained in good to excellent...
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Veröffentlicht in: | ACS catalysis 2017-06, Vol.7 (6), p.3763-3767 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The asymmetric synthesis of γ-alkenyl butenolides was accomplished by conjugated addition of butenolides to alkynones. Both terminal alkynones and nonterminal alkynones were applicable to the N,N′-dioxide–scandium(III) catalytic system. The corresponding products were obtained in good to excellent yields (up to 99%) with high E/Z ratios and high enantioselectivities (up to 98% ee). The novel methods of building both γ-alkenyl butenolides and continuing epoxidation products facilitated constructing core structure of biologically active natural products and synthetic intermediates. Additionally, one-pot Michael addition/epoxidation performed well with our catalytic system. |
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ISSN: | 2155-5435 2155-5435 |
DOI: | 10.1021/acscatal.7b00590 |