Synthesis and reactivity of bicycles derived from tartaric acid and α- amino acids: A novel class of conformationally constrained dipeptide isosteres based upon enantiopure 3-aza-6,8-dioxabicyclo[3.2.1] octane-7- carboxylic acid

Journal of Organic Chemistry

Volumn 64, Issue 20, 1999, Pages 7347-7364

  Guarna, Antonio ^a   Guidi, Antonio ^b   Machetti, Fabrizio ^a   Menchi, Gloria ^a   Occhiato, Ernesto G ^a   Scarpi, Dina ^a   Sisi, Sauro ^a   Trabocchi, Andrea ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

^b Menarini Ricerche SpA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; CARBOXYLIC ACID DERIVATIVE; DIPEPTIDE; TARTARIC ACID;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONFORMATION; ENANTIOMER; OXIDATION; PEPTIDE SYNTHESIS; STRUCTURE ANALYSIS;

EID: 0033214144     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9904967     Document Type: Article

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