Home Chemistry Heterocyclic Building Blocks Thiazolidines Thiazolidine
Ring Opening Reactions: Thiazolidine can undergo ring-opening reactions with nucleophiles or electrophiles. For example, it can react with strong nucleophiles to open the ring and form products with an open-chain structure.
Oxidation: Thiazolidine compounds can be oxidized under certain conditions. This can result in the formation of sulfoxides or sulfones, depending on the extent of oxidation.
Substitution Reactions: Thiazolidine can undergo nucleophilic substitution reactions when appropriate electrophiles are present. For instance, the thiazolidine ring can be substituted by a nucleophile to form various derivatives.
Reductive Cleavage: Thiazolidine can be cleaved under reductive conditions. This may lead to the formation of products with a reduced sulfur atom.
Alkylation or Acylation: Thiazolidine compounds can be alkylated or acylated by suitable reagents under appropriate conditions.
Cyclization Reactions: Thiazolidine compounds can participate in intramolecular cyclization reactions when suitable functional groups are present within the molecule.
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(R)-Ethyl thiazolidine-4-carboxylate hydrochloride
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(R)-Thiazolidine-4-carbonitrile hydrochloride
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(S)-3-(tert-Butoxycarbonyl)thiazolidine-2-carboxylic acid
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