Batch vs Continuous‐Flow Method to Synthesize N ‐(3‐Acylamidopropyl)Lactams Through N−C Bond Cleavage in Amides with Amidines von Govindan, Karthick, Chen, Nian‐Qi, Venkatachalam, Gokulakannan, Leung, Tsz‐Fai, Lin, Wei‐Yu

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Base-promoted triple cleavage of CCl 2 Br: a direct one-pot synthesis of unsymmetrical oxalamide derivatives von Jayaram, Alageswaran, Seenivasan, Vijay Thavasianandam, Govindan, Karthick, Liu, Yu-Ming, Chen, Nian-Qi, Yeh, Ting-Wei, Venkatachalam, Gokulakannan, Li, Chien-Hung, Leung, Tsz-Fai, Lin, Wei-Yu

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Base-promoted triple cleavage of CClBr: a direct one-pot synthesis of unsymmetrical oxalamide derivatives von Jayaram, Alageswaran, Seenivasan, Vijay Thavasianandam, Govindan, Karthick, Liu, Yu-Ming, Chen, Nian-Qi, Yeh, Ting-Wei, Venkatachalam, Gokulakannan, Li, Chien-Hung, Leung, Tsz-Fai, Lin, Wei-Yu

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Transition‐Metal Catalyzed Synthesis of N‐Heterocycles using Solvent‐Carbon (C1) Synthons von Govindan, Karthick, Jayaram, Alageswaran, Seenivasan, Vijay Thavasianandam, Venkatachalam, Gokulakannan, Lin, Wei‐Yu

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Base-promoted triple cleavage of CCl2Br: a direct one-pot synthesis of unsymmetrical oxalamide derivatives von Jayaram, Alageswaran, Seenivasan, Vijay Thavasianandam, Govindan, Karthick, Yu-Ming, Liu, Nian-Qi Chen, Ting-Wei Yeh, Venkatachalam, Gokulakannan, Chien-Hung, Li, Leung, Tsz-Fai, Wei-Yu, Lin

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