Thiophilic ring opening reactions of 3,3-bis(trifluoromethyl)-5-alkoxy-1,2-dithiolanes under action of nucleophiles - ScienceDirect
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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
Scheme 1. Reagent and conditions: i) 2.5 M n-BuLi, B(OMe)3, −78 o C;... | Download Scientific Diagram
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1,3-Dithiolanes, 1,3-Dithianes
Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene | Journal of the American Chemical Society
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![Low temperature n-butyllithium-induced [3,3]-sigmatropic rearrangement/electrophile trapping reactions of allyl-1,1-dichlorovinyl ethers. Synthesis of β-, γ- and δ-lactones - Organic & Biomolecular Chemistry (RSC Publishing)](https://pubs.rsc.org/en/Content/Image/GA/C3OB41777H "Low temperature n-butyllithium-induced [3,3]-sigmatropic rearrangement/electrophile trapping reactions of allyl-1,1-dichlorovinyl ethers. Synthesis of β-, γ- and δ-lactones - Organic & Biomolecular Chemistry (RSC Publishing)")
Low temperature n-butyllithium-induced [3,3]-sigmatropic rearrangement/electrophile trapping reactions of allyl-1,1-dichlorovinyl ethers. Synthesis of β-, γ- and δ-lactones - Organic & Biomolecular Chemistry (RSC Publishing)
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Asymmetric Deprotonation using s-BuLi or i-PrLi and Chiral Diamines in THF: The Diamine Matters | Journal of the American Chemical Society
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