![n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja068057u/asset/images/large/ja068057un00001.jpeg)
n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society
![n-Butyllithium, 1.6M solution in hexanes, AcroSeal , Thermo Scientific Chemicals, Quantity: 100 mL | Fisher Scientific n-Butyllithium, 1.6M solution in hexanes, AcroSeal , Thermo Scientific Chemicals, Quantity: 100 mL | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/CCG/Chemical-Structures/chemical-structure-cas-109-72-8.jpg-650.jpg)
n-Butyllithium, 1.6M solution in hexanes, AcroSeal , Thermo Scientific Chemicals, Quantity: 100 mL | Fisher Scientific
![Lithium diisopropylamide is a strong base and nonnucleophilic base. It is often freshly prepared by treating a certain reactant with n-butyllithium (n -BuLi). Draw the starting material and draw the product (lithium diisopropylamide). Lithium diisopropylamide is a strong base and nonnucleophilic base. It is often freshly prepared by treating a certain reactant with n-butyllithium (n -BuLi). Draw the starting material and draw the product (lithium diisopropylamide).](https://homework.study.com/cimages/multimages/16/imggg18985099675782387668.png)
Lithium diisopropylamide is a strong base and nonnucleophilic base. It is often freshly prepared by treating a certain reactant with n-butyllithium (n -BuLi). Draw the starting material and draw the product (lithium diisopropylamide).
![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 BuLi-promoted anti -Markovnikov selective hydroboration of unactivated alkenes and internal alkynes - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00750D n BuLi-promoted anti -Markovnikov selective hydroboration of unactivated alkenes and internal alkynes - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00750D](https://pubs.rsc.org/image/article/2019/QO/c9qo00750d/c9qo00750d-s1_hi-res.gif)
n BuLi-promoted anti -Markovnikov selective hydroboration of unactivated alkenes and internal alkynes - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00750D
![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)