A straightforward synthesis of both enantiomers of allo-norcoronamic acids and allo-coronamic acids, by asymmetric Strecker reaction from alkylcyclopropanone acetals

Tetrahedron Asymmetry

Volumn 9, Issue 2, 1998, Pages 305-320

  Fadel, Antoine ^a   Khesrani, Aballache ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CORONAMIC ACID; CYCLOPROPANECARBOXYLIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DIASTEREOISOMER; DRUG PURIFICATION; DRUG SYNTHESIS; ENANTIOMER; IN VITRO STUDY; METHODOLOGY; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0032579439     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00633-2     Document Type: Article

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46. It is interesting to note that the Strecker reaction can also occur directly from the acetal 7a or (±)-7b.
47. -1.
48. 3=77.00 ppm as a reference.