The compound (3R,4S)-1-[(tert-butoxy)carbonyl]-4-phenylpyrrolidine-3-carboxylic acid, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique molecular structure makes it a valuable reagent in the creation of various organic compounds.$name$ is frequently employed in the synthesis of complex molecules and pharmaceutical intermediates due to its chirality and reactive functional groups. Its carboxylic acid group allows for versatile derivatization and serves as a key site for further modification in organic reactions.In organic synthesis, (3R,4S)-1-[(tert-butoxy)carbonyl]-4-phenylpyrrolidine-3-carboxylic acid is utilized as a chiral auxiliary, enabling the stereocontrolled synthesis of enantiomerically enriched compounds. Its presence can dictate the stereochemistry of subsequent reactions, leading to the formation of desired chiral products with high selectivity.Additionally, $name$ can participate in various coupling reactions, such as amidation, esterification, and peptide bond formation, contributing to the construction of structurally diverse molecules. Its tert-butoxy carbonyl (Boc) protecting group can be selectively removed under mild conditions, allowing for further functional group manipulation.Overall, the application of (3R,4S)-1-[(tert-butoxy)carbonyl]-4-phenylpyrrolidine-3-carboxylic acid in chemical synthesis is instrumental in achieving stereochemical control, functional group diversity, and the efficient construction of complex organic molecules with diverse applications.
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(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
