![Rare Example of Nucleophilic Substitution at Vinylic Carbon with Inversion: Mechanism of Methyleneaziridine Formation by Sodium Amide Induced Ring Closure Revisited | Journal of the American Chemical Society Rare Example of Nucleophilic Substitution at Vinylic Carbon with Inversion: Mechanism of Methyleneaziridine Formation by Sodium Amide Induced Ring Closure Revisited | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja0482684/asset/images/medium/ja0482684h00001.gif)
Rare Example of Nucleophilic Substitution at Vinylic Carbon with Inversion: Mechanism of Methyleneaziridine Formation by Sodium Amide Induced Ring Closure Revisited | Journal of the American Chemical Society
![Bimolecular nucleophilic substitutions at the saturated sp 3 and vinyl... | Download Scientific Diagram Bimolecular nucleophilic substitutions at the saturated sp 3 and vinyl... | Download Scientific Diagram](https://www.researchgate.net/publication/228907258/figure/fig3/AS:667709901639702@1536205854578/Bimolecular-nucleophilic-substitutions-at-the-saturated-sp-3-and-vinyl-sp-2-carbon-atoms.png)
Bimolecular nucleophilic substitutions at the saturated sp 3 and vinyl... | Download Scientific Diagram
Radical 1,2,3-tricarbofunctionalization of α-vinyl-β-ketoesters enabled by a carbon shift from an all-carbon quaternary center - Chemical Science (RSC Publishing)
![Long-range coupling between protons more than two carbon atoms apart is sometimes observed when pi bonds intervene. An example is found in 1-methoxy-1-buten-3-yne. Not only does the acetylenic proton, Ha, couple with Long-range coupling between protons more than two carbon atoms apart is sometimes observed when pi bonds intervene. An example is found in 1-methoxy-1-buten-3-yne. Not only does the acetylenic proton, Ha, couple with](https://homework.study.com/cimages/multimages/16/1-methoxy-1-buten-3-yne5354684501555010693.png)
Long-range coupling between protons more than two carbon atoms apart is sometimes observed when pi bonds intervene. An example is found in 1-methoxy-1-buten-3-yne. Not only does the acetylenic proton, Ha, couple with
![Nucleophilic substitution at an sp2 carbon of vinyl halides with an intramolecular thiolate moiety: synthesis of 2-alkylidenethietanes - ScienceDirect Nucleophilic substitution at an sp2 carbon of vinyl halides with an intramolecular thiolate moiety: synthesis of 2-alkylidenethietanes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403908008083-gr2.jpg)