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- W4313889852 endingPage "668" @default.
- W4313889852 startingPage "668" @default.
- W4313889852 abstract "Azomethine ylides are nitrogen-based three-atom components commonly used in [3+2]-cycloaddition reactions with various unsaturated 2π-electron components. These reactions are highly regio- and stereoselective and have attracted the attention of organic chemists with respect to the construction of diverse heterocycles potentially bearing four new contiguous stereogenic centers. This review article complies the most important [3+2]-cycloaddition reactions of azomethine ylides with various olefinic, unsaturated 2π-electron components (acyclic, alicyclic, heterocyclic, and exocyclic ones) reported over the past two decades." @default.
- W4313889852 created "2023-01-10" @default.
- W4313889852 creator A5018294904 @default.
- W4313889852 creator A5084441438 @default.
- W4313889852 creator A5085989985 @default.
- W4313889852 creator A5091322050 @default.
- W4313889852 date "2023-01-09" @default.
- W4313889852 modified "2023-10-18" @default.
- W4313889852 title "Azomethine Ylides—Versatile Synthons for Pyrrolidinyl-Heterocyclic Compounds" @default.
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