Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi - Organic Chemistry Frontiers (RSC Publishing)
![organic chemistry - nBuLi and tBuLi can take part in halogen metal exchange OR deprotonate. Is there any way to predict which it favours? - Chemistry Stack Exchange organic chemistry - nBuLi and tBuLi can take part in halogen metal exchange OR deprotonate. Is there any way to predict which it favours? - Chemistry Stack Exchange](https://i.stack.imgur.com/Kw6gz.png)
organic chemistry - nBuLi and tBuLi can take part in halogen metal exchange OR deprotonate. Is there any way to predict which it favours? - Chemistry Stack Exchange
![n‐Butyllithium‐mediated reactions of 1‐(2‐azidoarylmethyl)‐ 1H‐benzotriazoles with alkyl halides - Kim - 2010 - Journal of Heterocyclic Chemistry - Wiley Online Library n‐Butyllithium‐mediated reactions of 1‐(2‐azidoarylmethyl)‐ 1H‐benzotriazoles with alkyl halides - Kim - 2010 - Journal of Heterocyclic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/611cea95-e3f3-4e32-951b-c9d6c6abdcde/mgra001.jpg)
n‐Butyllithium‐mediated reactions of 1‐(2‐azidoarylmethyl)‐ 1H‐benzotriazoles with alkyl halides - Kim - 2010 - Journal of Heterocyclic Chemistry - Wiley Online Library
![Regio- and stereoselective intermolecular carbolithiation reactions - RSC Advances (RSC Publishing) DOI:10.1039/D0RA06101H Regio- and stereoselective intermolecular carbolithiation reactions - RSC Advances (RSC Publishing) DOI:10.1039/D0RA06101H](https://pubs.rsc.org/image/article/2020/RA/d0ra06101h/d0ra06101h-s6_hi-res.gif)
Regio- and stereoselective intermolecular carbolithiation reactions - RSC Advances (RSC Publishing) DOI:10.1039/D0RA06101H
![Mechanism of the Deprotonation Reaction of Alkyl Benzyl Ethers with n‐ Butyllithium - Raposo - 2013 - Chemistry – A European Journal - Wiley Online Library Mechanism of the Deprotonation Reaction of Alkyl Benzyl Ethers with n‐ Butyllithium - Raposo - 2013 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/1c111562-9e54-4ef5-9e35-5976c2715f6c/msch003.jpg)
Mechanism of the Deprotonation Reaction of Alkyl Benzyl Ethers with n‐ Butyllithium - Raposo - 2013 - Chemistry – A European Journal - Wiley Online Library
![Scheme 2 Reagents and conditions: (i) TMS-acetylene, n BuLi, BF 3 ·Et 2... | Download Scientific Diagram Scheme 2 Reagents and conditions: (i) TMS-acetylene, n BuLi, BF 3 ·Et 2... | Download Scientific Diagram](https://www.researchgate.net/profile/Gerald-Pattenden-2/publication/38012699/figure/fig1/AS:394155588112392@1470985423581/Scheme-2-Reagents-and-conditions-i-TMS-acetylene-n-BuLi-BF-3-Et-2-O-78-to-30_Q320.jpg)
Scheme 2 Reagents and conditions: (i) TMS-acetylene, n BuLi, BF 3 ·Et 2... | Download Scientific Diagram
![Regio- and stereoselective intermolecular carbolithiation reactions - RSC Advances (RSC Publishing) DOI:10.1039/D0RA06101H Regio- and stereoselective intermolecular carbolithiation reactions - RSC Advances (RSC Publishing) DOI:10.1039/D0RA06101H](https://pubs.rsc.org/image/article/2020/RA/d0ra06101h/d0ra06101h-s14_hi-res.gif)
Regio- and stereoselective intermolecular carbolithiation reactions - RSC Advances (RSC Publishing) DOI:10.1039/D0RA06101H
![Been researching a synthesis, please can someone outline the mechanism for this step & are the butyllithium and thf reactants or used to dissolve the reactants or something : r/OrganicChemistry Been researching a synthesis, please can someone outline the mechanism for this step & are the butyllithium and thf reactants or used to dissolve the reactants or something : r/OrganicChemistry](https://preview.redd.it/5zs2hxto4r451.jpg?auto=webp&s=923b3dd9db5877ac63e234279255ba45cf08f402)
Been researching a synthesis, please can someone outline the mechanism for this step & are the butyllithium and thf reactants or used to dissolve the reactants or something : r/OrganicChemistry
![Unprecedented reactions: from epichlorohydrin to epoxyglycidyl substituted divinyl ether and its conversion into epoxyglycidyl propargyl ether | Scientific Reports Unprecedented reactions: from epichlorohydrin to epoxyglycidyl substituted divinyl ether and its conversion into epoxyglycidyl propargyl ether | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fsrep14231/MediaObjects/41598_2015_Article_BFsrep14231_Fig4_HTML.jpg)
Unprecedented reactions: from epichlorohydrin to epoxyglycidyl substituted divinyl ether and its conversion into epoxyglycidyl propargyl ether | Scientific Reports
![Mechanism of the Deprotonation Reaction of Alkyl Benzyl Ethers with n‐ Butyllithium - Raposo - 2013 - Chemistry – A European Journal - Wiley Online Library Mechanism of the Deprotonation Reaction of Alkyl Benzyl Ethers with n‐ Butyllithium - Raposo - 2013 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/d59c7d18-c035-45b0-ad12-415df18700d1/msch005.jpg)