Enantioselective synthesis of β-amino-diacids

Tetrahedron Letters

Volumn 46, Issue 47, 2005, Pages 8203-8205

  Alladoum, Jeanne ^a   Dechoux, Luc ^a  

^a SORBONNE UNIVERSITÉ   (France)

Author keywords

Amino acids; Amino diacids; Enaminolactone; (R) Phenylglycinol; Asymmetric synthesis

Indexed keywords

BETA AMINO ACID; CHLORINE DERIVATIVE; LACTONE DERIVATIVE; SODIUM DERIVATIVE;

ALKYLATION; ARTICLE; CHIRALITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOSELECTIVITY; STEREOCHEMISTRY;

EID: 27144442037     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.09.114     Document Type: Article

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41. 3, 62.9 MHz): 39.8, 53.1, 55.2, 62.1, 70.3, 87.7, 126.9, 127.6, 129.1, 129.2, 129.8, 137.4, 138.0, 152.0, 170.1, 172.7.
42. Atomic coordinates, bond lengths and angles have been deposited at the Cambridge Crystallographical Data Center with the deposition number CCDC283799.
43. Reductions were realized on diastereomerically- and enantiomerically pure compounds 4a,c and on a mixture of diastereoisomers of compound 4b.
44. 1H NMR spectroscopy (NOE experiments).
45. 3, 62.9 MHz): 34.8, 42.9, 52.3, 53.8, 54.3, 63.5, 75.4, 127.1, 127.2, 128.7, 129.0, 129.3, 129.4, 138.9, 140.2, 173.5, 174.1.
46. 3OD, 62.9 MHz): 36.4, 37.8, 51.1, 51.9, 52.9, 128.4, 130.1, 130.3, 139.1, 174.5, 176.