Cyclic (4 S)-chloromethyl sulfite and sulfate derivatives of ( S)-glycidol as valuable synthetic equivalents of scalemic epichlorohydrin
The interaction of ( S)-glycidol with SOCl 2 or SO 2Cl 2 in stoichiometric amounts leads to the formation of cyclic (4 S)-chloromethyl sulfite or sulfate derivatives with the same enantiomeric purity; based on this reaction, a new procedure for the synthesis of ( S)-propranolol was developed.
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Veröffentlicht in: | Mendeleev communications 1999, Vol.9 (6), p.236-237 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The interaction of (
S)-glycidol with SOCl
2 or SO
2Cl
2 in stoichiometric amounts leads to the formation of cyclic (4
S)-chloromethyl sulfite or sulfate derivatives with the same enantiomeric purity; based on this reaction, a new procedure for the synthesis of (
S)-propranolol was developed. |
---|---|
ISSN: | 0959-9436 |
DOI: | 10.1070/MC1999v009n06ABEH001190 |