Enantioselective Copper‐Catalyzed Formal [2+1] and [4+1] Annulations of Diynes with Ketones via Carbonyl Ylides

Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst‐controlled highly...

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Published inAngewandte Chemie International Edition Vol. 61; no. 43
Main Authors Qi, Lin‐Jun, Li, Cui‐Ting, Huang, Zheng‐Qi, Jiang, Jia‐Tian, Zhu, Xin‐Qi, Lu, Xin, Ye, Long‐Wu
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 24.10.2022
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Abstract Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst‐controlled highly enantioselective reaction of carbonyl ylides from metal carbenes is extremely challenging. Herein, we report a novel copper‐catalyzed asymmetric formal [2+1] and [4+1] annulations of diynes with ketones via carbonyl ylides. Importantly, this protocol not only represents the first example of successful asymmetric epoxidation via carbonyl ylides, but also constitutes the first reaction of vinyl cations with carbonyl compounds. This method leads to the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities via remote‐stereocontrol strategy. A copper‐catalyzed asymmetric formal [2+1] and [4+1] annulation of diynes with ketones via carbonyl ylides is disclosed. This protocol enables the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities.
AbstractList Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O-heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst-controlled highly enantioselective reaction of carbonyl ylides from metal carbenes is extremely challenging. Herein, we report a novel copper-catalyzed asymmetric formal [2+1] and [4+1] annulations of diynes with ketones via carbonyl ylides. Importantly, this protocol not only represents the first example of successful asymmetric epoxidation via carbonyl ylides, but also constitutes the first reaction of vinyl cations with carbonyl compounds. This method leads to the divergent, practical and atom-economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities via remote-stereocontrol strategy.
Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst‐controlled highly enantioselective reaction of carbonyl ylides from metal carbenes is extremely challenging. Herein, we report a novel copper‐catalyzed asymmetric formal [2+1] and [4+1] annulations of diynes with ketones via carbonyl ylides. Importantly, this protocol not only represents the first example of successful asymmetric epoxidation via carbonyl ylides, but also constitutes the first reaction of vinyl cations with carbonyl compounds. This method leads to the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities via remote‐stereocontrol strategy. A copper‐catalyzed asymmetric formal [2+1] and [4+1] annulation of diynes with ketones via carbonyl ylides is disclosed. This protocol enables the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities.
ArticleNumber 202210637
Author Qi, Lin‐Jun
Huang, Zheng‐Qi
Jiang, Jia‐Tian
Lu, Xin
Li, Cui‐Ting
Zhu, Xin‐Qi
Ye, Long‐Wu
Author_xml – sequence: 1
  givenname: Lin‐Jun
  surname: Qi
  fullname: Qi, Lin‐Jun
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  fullname: Li, Cui‐Ting
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  givenname: Xin
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  surname: Ye
  fullname: Ye, Long‐Wu
  email: longwuye@xmu.edu.cn
  organization: Chinese Academy of Sciences
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Issue 43
Keywords Heterocycles
CARBENOIDS
REACTIVITY
ALDEHYDES
EPOXIDATION
CYCLOADDITION
EPOXIDES
YNAMIDES
Asymmetric Catalysis
Carbonyl Ylides
GENERATION
Annulation
ACCESS
Alkynes
DIHYDROFURANS
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Snippet Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by...
Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O-heterocycles, and the formation of carbonyl ylides by...
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SubjectTerms Alkynes
Annulation
Asymmetric Catalysis
Asymmetry
Carbenes
Carbonyl compounds
Carbonyl Ylides
Carbonyls
Catalysts
Cations
Chemistry
Chemistry, Multidisciplinary
Copper
Divergence
Enantiomers
Epoxidation
Heterocycles
Ketones
Physical Sciences
Science & Technology
Title Enantioselective Copper‐Catalyzed Formal [2+1] and [4+1] Annulations of Diynes with Ketones via Carbonyl Ylides
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202210637
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