Enantioselective construction of functionalized oxazoles <i>via</i> anionic stereogenic-at-cobalt(<scp>iii</scp>) complex-catalyzed Ugi-4CR/Wittig reaction sequences

A one-pot synthesis of chiral multifunctional oxazole frameworks is accomplished <i>via</i> a cascade reaction involving an anionic stereogenic cobalt(III) complex-catalyzed enantioselective Ugi four-component/Wittig process. This approach tolerates a complex reaction system that includes aldehydes, amines, carboxylic acids, and isocyano-(triphenylphosphoranylidene)acetates, yielding chiral 2,4,5-trisubstituted oxazoles with good enantioselectivities (up to 93 : 7 er).

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00293a
Citations
2
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
1.87
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article

Enantioselective construction of functionalized oxazoles via anionic stereogenic-at-cobalt(iii) complex-catalyzed Ugi-4CR/Wittig reaction sequences

Hua‐Jie Jiang, Cong Peng, Chuan‐Zhi Yao, Jie Yu et al.
2 citations
Organic & Biomolecular Chemistry
Asymmetric Synthesis and Catalysis
1.87
article

Enantioselective construction of functionalized oxazoles via anionic stereogenic-at-cobalt(iii) complex-catalyzed Ugi-4CR/Wittig reaction sequences

Hua‐Jie Jiang, Cong Peng, Chuan‐Zhi Yao, Jie Yu, Qiming Wang, Yunlan Sun
article en
2 citations

Abstract

A one-pot synthesis of chiral multifunctional oxazole frameworks is accomplished <i>via</i> a cascade reaction involving an anionic stereogenic cobalt(III) complex-catalyzed enantioselective Ugi four-component/Wittig process. This approach tolerates a complex reaction system that includes aldehydes, amines, carboxylic acids, and isocyano-(triphenylphosphoranylidene)acetates, yielding chiral 2,4,5-trisubstituted oxazoles with good enantioselectivities (up to 93 : 7 er).

Organic & Biomolecular ChemistryVol. 23(17)
Anhui Agricultural University (CN)
Openalex Percentile: Top 17%
Asymmetric Synthesis and Catalysis
1.87
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