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Nickel-Catalyzed Selective Monoamination of 1,2-Diols: An Affordable Approach to Amino Alcohols
Cite Jump to ExpandCollapse LetterAugust 21, 2025 Nickel-Catalyzed Selective Monoamination of 1,2-Diols: An Affordable Approach to Amino Alcohols Click to copy article linkArticle link copied! Soumya Sree Samal Soumya Sree Samal Department of Chemistry, Indian Institute of Science Education and Research (IISER) Tirupati, Tirupati 517619, India Murugan Subaramanian Murugan Subaramanian Department of Chemistry, Indian Institute of Science Education and Research (IISER) Tirupati, Tirupati...
Nickel catalyzed tandem conversion of paraformaldehyde:methanol to hydrogen and formate/chemo- and stereoselective hydrogenation of alkynes under neutral conditions
Nickel catalyzed tandem conversion of paraformaldehyde:methanol to hydrogen and formate/chemo- and stereoselective hydrogenation of alkynes under neutral conditions Development of new catalytic protocols for clean and COx-free hydrogen generation from fundamental feedstocks is always interesting and challenging. Herein, we disclose nickel-catalyzed dihydrogen generation from a mixture of paraformaldehyde-methanol under base-free and activator-free conditions.
Transition metal-catalysis in interrupted borrowing hydrogen strategy
Transition metal-catalysis in interrupted borrowing hydrogen strategy Madhu Nallagangula, a Murugan Subaramanian,a Rohit Kumara and Ekambaram Balaraman *a Abstract In recent times, the transition metal-catalyzed borrowing hydrogen (BH) and interrupted borrowing hydrogen (IBH) strategies have attracted much attention and represent atom- and step-economic processes to access diverse building blocks via various C–C and C–heteroatom bond-forming reactions.
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