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Structure of 13500-53-3
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This chiral pyrrolidine derivative features a dibenzyl-protected 4-hydroxypyrrolidine scaffold with defined stereochemistry at the 2S,4R positions. The molecule integrates a hydroxyl group and two benzyl ester functionalities, enabling selective deprotection and downstream coupling in asymmetric synthesis. Bench-stable and compatible with standard peptide and small-molecule workflows, it serves as a high-fidelity building block for complex natural product and pharmaceutical intermediates.
(2S,4R)-Dibenzyl 4-hydroxypyrrolidine-1,2-dicarboxylate serves as a stereochemically defined chiral building block for the synthesis of pyrrolidine-based scaffolds. The protected hydroxyl and dibenzyl ester functionalities enable selective transformations, including deprotection, derivatization, and coupling reactions. Its stability under standard bench conditions and compatibility with diverse reaction protocols facilitate efficient access to complex heterocycles and bioactive molecules in medicinal chemistry and process development workflows.
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Lot numbers can be found on the outside label of a product: