Cycloaddition of a chiral nitrone to allylic motifs: An access to enantiopure sugar-based amino acids displaying a stable glycosidic bond and to 4(S)-4-hydroxy-l-ornithine

Tetrahedron

Volumn 68, Issue 6, 2012, Pages 1762-1768

  Aouadi, Kaïss ^a,b,c,d   Msaddek, Moncef ^c   Praly, Jean Pierre ^a,b  

^a UNIVERSITÉ LYON 1   (France)

^b CPE LYON   (France)

^c FACULTÉ DES SCIENCES DE MONASTIR   (Tunisia)

^d ISSAT   (Tunisia)

Author keywords

( ) Menthone; Chiral nitrone; Diastereoselective cycloaddition; Isoxazolidines; N O bond reductive cleavage; Sugar based amino acids

Indexed keywords

ALLYL COMPOUND; AMINO ACID DERIVATIVE; ARGININE DERIVATIVE; GLYCOSIDE; GUANIDINE DERIVATIVE; MENTHONE; NITRONE; ORNITHINE DERIVATIVE; SUGAR;

ACIDITY; ALKALINITY; ARTICLE; CHEMICAL BOND; CHIRALITY; CYCLOADDITION; ENANTIOMER; HYDROLYSIS; PRIORITY JOURNAL; QUANTUM YIELD; REACTION ANALYSIS; RING OPENING;

EID: 84855925238     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.12.048     Document Type: Article

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