A diastereoselective synthesis of the tetrahydropyridazinone core of 2-oxo-1,6-diazobicyclo[4.3.0]nonane-9-carboxylate-based peptidomimetics starting from (S)-phenylalanine

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dc.contributor.authorGardiner, J.
dc.contributor.authorAbell, A.
dc.date.issued2003
dc.description.abstractA diastereoseletvive synthesis of a peptidic tetrahydropyridazinone 10 from (S)-phenylalanine is reported. This derivative was then converted to the bicyclic peptidomimetic 11, an important class of β-strand mimetic. © 2003 Elsevier Science Ltd. All rights reserved.
dc.description.statementofresponsibilityJames Gardiner and Andrew D. Abell
dc.identifier.citationTetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 2003; 44(22):4227-4230
dc.identifier.doi10.1016/S0040-4039(03)00882-7
dc.identifier.issn0040-4039
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]
dc.identifier.urihttp://hdl.handle.net/2440/34469
dc.language.isoen
dc.publisherPergamon-Elsevier Science Ltd
dc.source.urihttps://doi.org/10.1016/s0040-4039(03)00882-7
dc.titleA diastereoselective synthesis of the tetrahydropyridazinone core of 2-oxo-1,6-diazobicyclo[4.3.0]nonane-9-carboxylate-based peptidomimetics starting from (S)-phenylalanine
dc.typeJournal article
pubs.publication-statusPublished

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