Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/90774
Title: One-pot diastereoselective synthesis of chiral tricyclic L-cysteine and D-penicillamine derivatives: a laboratory experiment
Authors: Soares, Maria I. L. 
Lopes, Susana M. M. 
Murtinho, Dina 
Pinho e Melo, Teresa M. V. D. 
Keywords: Organic chemistry; Heterocycles; Thiazolidine; Diastereoselective synthesis; Chiral pool; NMR spectroscopy
Issue Date: 21-Nov-2019
Publisher: Sociedade Brasileira de Química
Project: UID/QUI/00313/2019 
Serial title, monograph or event: química nova
Volume: 43
Issue: 1
Abstract: A one-pot diastereoselective synthesis of thiazolidine-ring fused systems derived from enantiomerically pure amino acids, L-cysteine or D-penicillamine, and achiral succindialdehyde is described as an experiment to be carried out by upper-division undergraduate students in a laboratory classroom. Reactions were performed under mild conditions, the products were isolated through simple experimental procedures and fully characterized. This study combines organic synthesis, determination of the purity of compounds (TLC analysis and melting point measurements), optical activity measurements as well as structural analysis (interpretation of 1D NMR and 2D NMR spectra). It offers a platform for the discussion of important organic chemistry concepts such as diastereoselectivity, kinetic control vs thermodynamic control and cyclization reactions via nucleophilic addition to imines/iminium cations.
URI: http://hdl.handle.net/10316/90774
ISSN: 0100-4042
1678-7064 (online)
DOI: 10.21577/0100-4042.20170448
Rights: openAccess
Appears in Collections:I&D CQC - Artigos em Revistas Internacionais

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