The compound 3,4,5-Piperidinetriol, 2-methyl-, (2S,3R,4S,5R), is a versatile chiral building block that finds wide application in chemical synthesis. Its unique structure, with multiple hydroxyl groups and a methyl substituent on the piperidine ring, allows for various synthetic pathways and transformations to be carried out.One of the key applications of 3,4,5-Piperidinetriol, 2-methyl-, (2S,3R,4S,5R), is as a starting material for the synthesis of complex natural products and pharmaceutical intermediates. The chiral nature of the molecule, with defined stereochemistry at multiple positions, makes it particularly valuable in the construction of enantiomerically pure compounds.In chemical synthesis, this compound can serve as a building block for the creation of diverse molecular structures through reactions such as acylation, alkylation, and cross-coupling. Its presence of hydroxyl groups also offers the potential for further derivatization, enabling the introduction of additional functional groups for fine-tuning the properties of the final product.Overall, the strategic incorporation of 3,4,5-Piperidinetriol, 2-methyl-, (2S,3R,4S,5R), in chemical synthesis allows chemists to access a range of complex molecules with precise stereochemical control and functional group diversity.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
