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Directed ortho-metalation–nucleophilic acyl substitution strategies in deep eutectic solvents: the organolithium base dictates the chemoselectivity

机译：深红色溶剂中指导的正交 - 金属化 - 亲核酰基取代策略：有机锂基础决定了化学选择性

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Simone Ghinato; Giuseppe Dilauro; Filippo Maria Perna; Vito Capriati; Marco Blangetti; Cristina Prandi;
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机译：开发深共晶溶剂和有机锂试剂的伙伴关系：在有氧环境温度条件下，亚胺和喹啉的化学选择性超快加成
2. Exploiting Deep Eutectic Solvents and Organolithium Reagent Partnerships: Chemoselective Ultrafast Addition to Imines and Quinolines Under Aerobic Ambient Temperature Conditions [J] . Vidal Cristian, Garcia-Alvarez Joaquin, Hernan-Gomez Alberto, Angewandte Chemie . 2016,第52期

机译：开发深共晶溶剂和有机锂试剂的伙伴关系：在有氧环境温度条件下，亚胺和喹啉的化学选择性超快加成
3. Application of Organolithium and Related Reagents in Synthesis; Part 26.~1 Synthetic Strategies Based on Directed ortho-Metalation: Synthesis of 4-Methyl-2H-phthalazin-1-ones [J] . Jan Epsztajn, Zbigniew Malinowski, jacek Z. Brzezinki, Synthesis: International Journal of Methods in Synthetic Organic Chemistry . 2001,第14期

机译：有机锂及相关试剂在合成中的应用;第26.〜1部分基于定向邻位金属化的合成策略：4-甲基-2H-酞嗪-1-酮的合成
4. Degummed palm oil methanolysis process using Choline Chloride (ChCl) and glycerol based Deep Eutectic Solvent (DES) as co-solvent at biodiesel production [C] . Renita Manurung, Ardian Syahputra, Muhammad Arif Alhamdi, International Conference on Sustainable Energy Engineering nd Application . 2017

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机译：第1部分：通过分子内亚甲基转移的三氟甲磺酸镧（III）催化的环丙烷化作用第2部分：与芳香族离子的反应设计-亲核酰基取代和有机光氧化还原催化剂。
6. Sustainable Asymmetric Organolithium Chemistry: Enantio‐ and Chemoselective Acylations through Recycling of Solvent Sparteine and Weinreb Amine [O] . Serena Monticelli, Wolfgang Holzer, Thierry Langer, -1

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7. Exploiting Deep Eutectic Solvents and Organolithium Reagent Partnerships: Chemoselective Ultrafast Addition to Imines and Quinolines Under Aerobic Ambient Temperature Conditions [O] . Vidal Vides, Cristian, García Álvarez, Joaquín, Hernán-Gómez, A., 2016

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Directed ortho-metalation–nucleophilic acyl substitution strategies in deep eutectic solvents: the organolithium base dictates the chemoselectivity

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