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a non-polar solvent; used frequently as a building block in organic chemistry Carbon tetrachloride: toxic, and its dissolving power is low; consequently, it has been largely superseded by deuterated solvents: Carbonyldiimidazole: often used for the coupling of amino acids for peptide synthesis and as a reagent in organic synthesis Ceric ...
Organic synthesis is an important chemical process that is integral to many scientific fields. Examples of fields beyond chemistry that require organic synthesis include the medical industry, pharmaceutical industry, and many more. Organic processes allow for the industrial-scale creation of pharmaceutical products.
Bischler–Möhlau indole synthesis; Bischler–Napieralski reaction; Biuret test; Blaise ketone synthesis; Blaise reaction; Blanc reaction; Blanc chloromethylation; Blum–Ittah aziridine synthesis; Bodroux reaction; Bodroux–Chichibabin aldehyde synthesis; Bogert–Cook synthesis; Bohlmann-Rahtz pyridine synthesis; Bohn–Schmidt reaction ...
Computer-assisted organic synthesis software is a type of application software used in organic chemistry in tandem with computational chemistry to help facilitate the tasks of designing, predicting, and producing chemical reactions. CAOS aims to identify a series of chemical reactions which, from a starting compound, can produce a desired molecule.
The following outline is provided as an overview of and topical guide to organic chemistry: . Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.
Total synthesis targets can also be organometallic or inorganic. [5] [6] While total synthesis aims for complete construction from simple starting materials, modifying or partially synthesizing these compounds is known as semisynthesis. Natural product synthesis serves as a critical tool across various scientific fields.
Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).
A name reaction (or named reaction) is a chemical reaction named after its discoverer(s) or developer(s). Among the tens of thousands of organic reactions that are known, hundreds of such reactions are typically identified by the eponym. [1]