Synthesis of highly oxygenated bicyclo[4.3.0]nonanes from sugar allyltins: model transformations of the adduct derived from the d-mannose

Tetrahedron Asymmetry

Volumn 19, Issue 9, 2008, Pages 1127-1133

  Jarosz, Sławomir ^a   Błońska, Anna ^a   Cmoch, Piotr ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

2 AZIDO 2 DEOXY 3 HYDROXY 7,8,9 TRI O BENZYL 5 BENZYLOXYBICYCLO[4.3.0]NONANE; 2,3 DI HYDROXY 7,8,9 TRI O BENZYL 5 BENZYLOXYMETHYLBICYCLO[4.3.0]NONANE; 3 AZIDO 3 DEOXY 2 HYDROXY 7,8,9 TRI O BENZYL 5 BENZYLOXYMETHYLBICYCLO[4.3.0]NONANE; 7,8,9 TRI O BENZYL 2,3 EPOXY 5 BENZYLOXYMETHYLBICYCLO[4.3.0]NONANE; 7,8,9 TRI O BENZYLOXYMETHYLBICYCLO[4.3.0]NON 2 ENE; ALLYLTIN DERIVATIVE; BICYCLO COMPOUND; CARBOHYDRATE DERIVATIVE; EPOXIDE; MANNOSE; NONANE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; DIELS ALDER REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 43649096286     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.04.014     Document Type: Article

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