The iodolactone approach to enantiopure oxiranes of constrained chiral cyclic β-amino acids

Tetrahedron Asymmetry

Volumn 19, Issue 18, 2008, Pages 2135-2139

  Songis, Olivier ^a   Didierjean, Claude ^b   Martinez, Jean ^a   Calmès, Monique ^a  

^a UNIV MONTPELLIER   (France)

^b Nancy University CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BENZOIC ACID DERIVATIVE; BETA AMINO ACID; ETHYLENE OXIDE DERIVATIVE; LACTONE DERIVATIVE;

ALKALINITY; ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; DEIODINATION; METHODOLOGY; PRIORITY JOURNAL; SEPARATION TECHNIQUE; STEREOCHEMISTRY; SYNTHESIS;

EID: 53649086311     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.09.005     Document Type: Article

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56. 13C spectra were observed for the two epoxides obtained with mCPBA. For example, 6-H, 3-H and 2-H chemical shifts were, respectively, 2.66 ppm (dd), 3.32 ppm (t) and 3.51 ppm (d) for the major epoxide and 2.90 ppm (d), 4.05 ppm (d) and 4.57 ppm (s) for the minor epoxide.
57. *The NMR of this compound is complicated by the presence of carbamate rotamers.)