Highly regioselective lithiation of pyridines bearing an oxetane unit by n- butyllithium - Chemical Communications (RSC Publishing)
![Acros Organics AC187540090 sec-Butyllithium, 1.3M solution in cyclohexane/hexane (92/8) (9g) from Cole-Parmer India Acros Organics AC187540090 sec-Butyllithium, 1.3M solution in cyclohexane/hexane (92/8) (9g) from Cole-Parmer India](https://pim-resources.coleparmer.com/item/l/acros-organics-ac187540090-sec-butyllithium-1-3m-solution-in-cyclohexane-hexane-92-8-9g-8820046.jpg)
Acros Organics AC187540090 sec-Butyllithium, 1.3M solution in cyclohexane/hexane (92/8) (9g) from Cole-Parmer India
Ministry of Chemistry - n-#Butyllithium (abbreviated #nBuLi) is an organolithium reagent. It is widely used as a polymerization initiator in the production of elastomers such as #polybutadiene or styrene-butadiene-styrene (#SBS). Also, it
![SOLVED: Match the species below to their appropriate, relative basic strength. butyllithium acetate alkoxide acetate Weakest Base alkoxide 2) Medium strength base 3) Strongest Base butyllithium SOLVED: Match the species below to their appropriate, relative basic strength. butyllithium acetate alkoxide acetate Weakest Base alkoxide 2) Medium strength base 3) Strongest Base butyllithium](https://cdn.numerade.com/ask_images/81f1f3481f9749b184d08fb9b44b7262.jpg)
SOLVED: Match the species below to their appropriate, relative basic strength. butyllithium acetate alkoxide acetate Weakest Base alkoxide 2) Medium strength base 3) Strongest Base butyllithium
![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
Effect of Solvent on the Lithium−Bromine Exchange of Aryl Bromides: Reactions of n-Butyllithium and tert-Butyllithium with 1-Bromo-4-tert-butylbenzene at 0 °C | The Journal of Organic Chemistry
![n-Butyllithium-promoted regioselective elimination of vicinal bis-triflate having an adjacent ether oxygen - ScienceDirect n-Butyllithium-promoted regioselective elimination of vicinal bis-triflate having an adjacent ether oxygen - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403917311620-fx1.jpg)