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For example, the synthesis of paracetamol typically requires three separate reactions. Divergent synthesis starts with a common intermediate, which branches into multiple final products through distinct reaction pathways. Convergent synthesis synthesis involves the combination of multiple intermediates synthesized independently to create a ...
In a combinatorial synthesis, when using only single starting material, it is possible to synthesize a large library of molecules using identical reaction conditions that can then be screened for their biological activity. This pool of products is then split into three equal portions containing each of the three products, and then each of the ...
One example of a synthesis reaction is the combination of iron and sulfur to form iron(II) sulfide: + Another example is simple hydrogen gas combined with simple oxygen gas to produce a more complex substance, such as water.
The Ugi reaction has been applied in combination with an intramolecular Diels-Alder reaction [16] in an extended multistep reaction. A reaction in its own right is the Ugi–Smiles reaction with the carboxylic acid component replaced by a phenol. In this reaction the Mumm rearrangement in the final step is replaced by the Smiles rearrangement. [17]
Suppose the yield is 50% for each reaction; the overall yield of D is only 12.5% from A. In a convergent synthesis A → B (50%) C → D (50%) B + D → E (25%) the overall yield of E (25%) looks much better. Convergent synthesis is applied in the synthesis of complex molecules and involves fragment coupling and independent synthesis. This ...
The reaction may otherwise involve the functional groups of the molecule, and is a versatile class of reactions that can occur in acidic or basic conditions or in the presence of a catalyst. This class of reactions is a vital part of life as it is essential to the formation of peptide bonds between amino acids and to the biosynthesis of fatty ...
The overall reaction type is a combination of both an addition reaction as well as a rearrangement reaction. This reaction was discovered by Max Conrad (1848–1920) and Leonhard Limpach (1852–1933) in 1887 while they were studying the synthesis of quinoline derivatives. [1] [2] The Conrad-Limpach synthesis
In the example below the carbonyl group in benzaldehyde is activated by diboronic acid prior to reaction with the allyl alcohol (see: Prins reaction): [4] The active catalyst system in this reaction is a combination of a palladium pincer compound and p-toluenesulfonic acid, the reaction product is obtained as a single regioisomer and stereoisomer.