The 1,3‐Dipolar Cycloaddition: From Conception to Quantum Chemical
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PDF) Recent advances in the photochemistry of the carbon-nitrogen double bond
Unveiling the high reactivity of experimental pseudodiradical azomethine ylides within molecular electron density theory - Physical Chemistry Chemical Physics (RSC Publishing) DOI:10.1039/D2CP05032C
Molecules, Free Full-Text
Diradical-singlet character of 1,3-dipoles affects reactivity of 1,3-dipolar cycloaddition reactions and intramolecular cyclization
Approach to a Substituted Heptamethine Cyanine Chain by the Ring Opening of Zincke Salts.
Molecular Electron Density Theory (MEDT) : Comments
Molecules, Free Full-Text
Unveiling the high reactivity of experimental pseudodiradical azomethine ylides within molecular electron density theory - Physical Chemistry Chemical Physics (RSC Publishing) DOI:10.1039/D2CP05032C
1,3-Dipolar Cycloadditions - Planning Organic Syntheses
BJOC - Search Results
Buy Trimethyl cyclopropane-1,2,3-tricarboxylate, 717-69-1
Fine-Tuning Strain and Electronic Activation of Strain-Promoted 1,3-Dipolar Cycloadditions with Endocyclic Sulfamates in SNO-OCTs. - Abstract - Europe PMC
The 1,3‐Dipolar Cycloaddition: From Conception to Quantum Chemical Design - Beutick - 2022 - Chemistry – An Asian Journal - Wiley Online Library
1, 3-Dipolar cycloaddition reactions of selected 1,3-dipoles with 7-isopropylidenenorbornadiene and follow-up thermolytic cleavage: A computational study - ScienceDirect
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