Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids

Autor:	Arvydas Stoncius, Norbert Sewald, Markus Nahrwold
Jazyk:	angličtina
Rok vydání:	2005
Předmět:	chemistry.chemical_classification Stereochemistry organic chemicals Organic Chemistry Regioselectivity ring closure Catalysis Amino acid beta-amino acids chemistry regioselectivity polycyclic compounds Organic chemistry rearrangements heterocyclic compounds Beta (finance) stereoselective synthesis
DOI:	10.1055/s-2005-865362
Popis:	Five suitably protected enantiomerically pure beta(2)-amino acids, homologues of proteinogenic alpha-amino acids, were synthesized from the common chiral precursor, tert-butyl succinyloxazolidinone.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d763a2d34bcfd04b96122ad79e351143 https://doi.org/10.1055/s-2005-865362 Zobrazit plný text záznamu