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pubmed-article:19795068pubmed:abstractTextSimple unmodified N-proline-based di- and tripeptides in combination with sodium hydroxide additive catalyze the asymmetric Michael reaction of ketones with nitroolefins to furnish the corresponding gamma-nitroketones with up to 99% yield, 99:1 dr and 70% ee at room temperature and on water without any organic cosolvent.lld:pubmed
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pubmed-article:19795068pubmed:articleTitleEnantioselective nitro-Michael reactions catalyzed by short peptides on water.lld:pubmed
pubmed-article:19795068pubmed:affiliationDepartment of Chemistry and Pharmacy, Institute of Organic Chemistry 1, University of Erlangen-Nuremberg, Henkestrasse 42, 91054, Erlangen, Germany.lld:pubmed
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