Recursive Chemical Reactions

<a href="https://www.rdkit.org/docs/Overview.html" rel="noopener ugc nofollow" target="_blank">RDKit </a>is an open-source cheminformatics toolkit written in C++ that can also be used in Java, Python, and <a href="https://www.knime.com/rdkit" rel="noopener ugc nofollow" target="_blank">KNIME</a>. It provides a wide collection of cheminformatics functionality, such as reading and writing molecules, working with atoms, bonds and rings, generating 2D or 3D coordinates, searching for substructures, applying chemical transformations, and computing fingerprints and descriptors. RDKit also offers a high-performance database <a href="https://www.rdkit.org/docs/Cartridge.html" rel="noopener ugc nofollow" target="_blank">cartridge</a> for PostgreSQL. RDKit understands <a href="https://www.daylight.com/dayhtml/doc/theory/theory.smarts.html" rel="noopener ugc nofollow" target="_blank">SMARTS</a>, the language for describing molecular patterns, and SMIRKS, the language for applying reaction transformations, both of which use as a basis SMILES, the famous line notation for entering and representing molecules and reactions. <a href="https://towardsdatascience.com/recursive-chemical-reactions-how-to-algorithmicallyanalyze-chemical-structures-c6a0fab95fa0">Read More</a>