![organic chemistry - Why does the unstabilised Wittig reaction selectively form cis alkenes? - Chemistry Stack Exchange organic chemistry - Why does the unstabilised Wittig reaction selectively form cis alkenes? - Chemistry Stack Exchange](https://i.stack.imgur.com/wNnDn.png)
organic chemistry - Why does the unstabilised Wittig reaction selectively form cis alkenes? - Chemistry Stack Exchange
![Scheme 8: Proposed mechanism for the base-free catalytic Wittig reaction. | Download Scientific Diagram Scheme 8: Proposed mechanism for the base-free catalytic Wittig reaction. | Download Scientific Diagram](https://www.researchgate.net/publication/329372860/figure/fig2/AS:722278262263812@1549215965898/Scheme-8-Proposed-mechanism-for-the-base-free-catalytic-Wittig-reaction_Q640.jpg)
Scheme 8: Proposed mechanism for the base-free catalytic Wittig reaction. | Download Scientific Diagram
![Tandem-, Domino- and One-Pot Reactions Involving Wittig- and Horner-Wadsworth-Emmons Olefination | IntechOpen Tandem-, Domino- and One-Pot Reactions Involving Wittig- and Horner-Wadsworth-Emmons Olefination | IntechOpen](https://www.intechopen.com/media/chapter/56853/media/F6.png)
Tandem-, Domino- and One-Pot Reactions Involving Wittig- and Horner-Wadsworth-Emmons Olefination | IntechOpen
![The modern interpretation of the Wittig reaction mechanism - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C3CS60105F The modern interpretation of the Wittig reaction mechanism - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C3CS60105F](https://pubs.rsc.org/image/article/2013/CS/c3cs60105f/c3cs60105f-s11.gif)
The modern interpretation of the Wittig reaction mechanism - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C3CS60105F
![Unequivocal Experimental Evidence for a Unified Lithium Salt-Free Wittig Reaction Mechanism for All Phosphonium Ylide Types: Reactions with β-Heteroatom-Substituted Aldehydes Are Consistently Selective for cis-Oxaphosphetane-Derived Products | Journal ... Unequivocal Experimental Evidence for a Unified Lithium Salt-Free Wittig Reaction Mechanism for All Phosphonium Ylide Types: Reactions with β-Heteroatom-Substituted Aldehydes Are Consistently Selective for cis-Oxaphosphetane-Derived Products | Journal ...](https://pubs.acs.org/cms/10.1021/ja300943z/asset/images/large/ja-2012-00943z_0010.jpeg)