Angewandte Chemie International Edition · 2001 · 9.3K citations · 128 references
PharmacyBiochemistryChemistryCombinatorial ChemistryDrug DiscoveryOrganic ChemistryChemical Library DesignCombinatorial SynthesisDiversity-oriented SynthesisHeterocyclic ChemistryMacromolecular AssemblyOrganic SynthesisAmino AcidsCarbon DioxideCarbon-heteroatom Bond FormationChemoselective Library SynthesisClick ChemistryCombinatorial Library ConstructionMacromolecule SynthesisSmall-molecule Library Construction
Examination of nature's favorite molecules reveals a striking preference for making carbon-heteroatom bonds over carbon-carbon bonds-surely no surprise given that carbon dioxide is nature's starting material and that most reactions are performed in water. Nucleic acids, proteins, and polysaccharides are condensation polymers of small subunits stitched together by carbon-heteroatom bonds. Even the 35 or so building blocks from which these crucial molecules are made each contain, at most, six contiguous C-C bonds, except for the three aromatic amino acids. Taking our cue from nature's approach, we address here the development of a set of powerful, highly reliable, and selective reactions for the rapid synthesis of useful new compounds and combinatorial libraries through heteroatom links (C-X-C), an approach we call "click chemistry". Click chemistry is at once defined, enabled, and constrained by a handful of nearly perfect "spring-loaded" reactions. The stringent criteria for a process to earn click chemistry status are described along with examples of the molecular frameworks that are easily made using this spartan, but powerful, synthetic strategy.
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The Atom Economy—A Search for Synthetic Efficiency
Catalytic asymmetric synthesis
Choice Reviews Online · 2001 · 2.7K citations
Thomas D. Penning, John J. Talley, Stephen R. Bertenshaw et al. · Journal of Medicinal Chemistry · 1997 · 2K citations · Full text