![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/a41508a9-c3af-4896-bfba-0657dbba50e0/mcontent.gif)
Mechanism of the Deprotonation Reaction of Alkyl Benzyl Ethers with n‐Butyllithium - Raposo - 2013 - Chemistry – A European Journal - Wiley Online Library
n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society
![Scheme 1. Different reactions of N, N-dimethylbenzylamine with n-BuLi /... | Download Scientific Diagram Scheme 1. Different reactions of N, N-dimethylbenzylamine with n-BuLi /... | Download Scientific Diagram](https://www.researchgate.net/publication/287635537/figure/fig1/AS:655350361489408@1533259110278/Scheme-1-Different-reactions-of-N-N-dimethylbenzylamine-with-n-BuLi-S-8-Reaction_Q320.jpg)
Scheme 1. Different reactions of N, N-dimethylbenzylamine with n-BuLi /... | Download Scientific Diagram
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n BuLi-promoted anti -Markovnikov selective hydroboration of unactivated alkenes and internal alkynes - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00750D
![NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/4aaa0691-61cb-47c0-99a9-f8aa4d87add9/anie202214106-toc-0001-m.jpg)