Stereoselective access to oc-azido aldehydes and a new synthetic route to myriocin

Bulletin de la Societe Chimique de France

Volumn 133, Issue 6, 1996, Pages 581-585

  Deloisy, Sandrine ^a   Thang, Ton That ^b   Olesker, Alain ^a   Lukacs, Gabor ^b  

^a INSTITUT DE CHIMIE DES SUBSTANCES NATURELLES   (France)

^b CNRS   (France)

Author keywords

Darzens' condensation; Immunosuppressant; Myriocin; Q azido aldehyde

Indexed keywords

EID: 0008071740     PISSN: 00378968     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (24)

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24. The discrepancy between our value and the reported [U]D value for 14b is due to a less precise measurement at lower concentration. The 1H-1H NMR Noesy experiment on 14a revealed a reversed signal assignment for H-3 and H-4 relative to the signal attribution proposed earlier [15]. For carbon numbering, see figure 1.