Highly diastereoselective synthetic route to enantiopure β2-amino acids and γ-amino alcohols using a fluorinated oxazolidine (Fox) as chiral auxiliary

Journal of Organic Chemistry

Volumn 73, Issue 10, 2008, Pages 3970-3973

  Tessier, Arnaud ^a   Lahmar, Nour ^a   Pytkowicz, Julien ^a   Brigaud, Thierry ^a  

^a Université Paris Seine   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; CHIRALITY; REACTION KINETICS; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

AMINO ALCOHOLS; DIASTEREOSELECTIVE SYNTHETIC ROUTE; ENANTIOPURE;

AMINO ACIDS;

AMINOALCOHOL; BETA AMINO ACID; FLUORINE; OXAZOLIDINE DERIVATIVE;

ALKYLATION; ARTICLE; BENZYLATION; CHEMICAL STRUCTURE; DERIVATIZATION; FLUORINATION; MANNICH REACTION; STEREOCHEMISTRY; SYNTHESIS;

AMINO ACIDS; AMINO ALCOHOLS; MOLECULAR CONFORMATION; OXAZOLES; STEREOISOMERISM;

EID: 43449104246     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800562x     Document Type: Article

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