An Expeditious Approach to Trisubstituted Chiral Tetrahydrofurans

An Expeditious Approach to Trisubstituted Chiral Tetrahydrofurans

Ozonolysis of 3,6-anhydro-4-0-(p-toluenesulphonyl)-D-glucal (9), obtained in four steps from D-glucose, provided the target compound 11. The structure and configurations of 9 and 11 have been determined by spectral studies and X-ray crystallography. Similar strategy with D-galactose provided the cor...

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Veröffentlicht in:Zeitschrift für Naturforschung. B, A journal of chemical sciences A journal of chemical sciences, 2000-04, Vol.55 (3), p.317-320
Hauptverfasser: Iqbal, Fazila, Shekhani, Mohammed Saleh, Malik, Abdul, Parvez, Masood, Riaz, Uzma, Ali, Zulfiqar, Khan, Khalid Mohammed
Format: Artikel
Sprache:eng
Schlagworte:
Asymmetric Synthesis
Chiral Tetrahydrofurans
D-Galactose
D-Glucose
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Zusammenfassung:Ozonolysis of 3,6-anhydro-4-0-(p-toluenesulphonyl)-D-glucal (9), obtained in four steps from D-glucose, provided the target compound 11. The structure and configurations of 9 and 11 have been determined by spectral studies and X-ray crystallography. Similar strategy with D-galactose provided the corresponding derivatives 10 and 12, respectively
ISSN:0932-0776
1865-7117
DOI:10.1515/znb-2000-3-413