Asymmetric synthesis of alkane- and arenesulfinates of diacetone-D-glucose (DAG) : an improved and general route to both enaniomerically pure sulfoxides
In: Journal of organic chemistry, Jg. 57 (1992), Heft 25, S. 6789-6796
Online
academicJournal
- print, 37 ref
Zugriff:
Diactone-D-glucose (DAG), a commercially available, sugar-derived secondary alcohol, was found to react with alkane- and arenesulfinyl chlorides in the presence of a tertiary amine in a very useful manner. When i-Pr2NEtis used as the base, (-)-(S)-alkane- and arenesulfinates are obtained in 50-90% yield with 89-≥95% de.
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Asymmetric synthesis of alkane- and arenesulfinates of diacetone-D-glucose (DAG) : an improved and general route to both enaniomerically pure sulfoxides
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Autor/in / Beteiligte Person: | FERNANDEZ, I ; KHIAR, N ; LLERA, J. M ; ALCUDIA, F |
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Zeitschrift: | Journal of organic chemistry, Jg. 57 (1992), Heft 25, S. 6789-6796 |
Veröffentlichung: | Washington, DC: American Chemical Society, 1992 |
Medientyp: | academicJournal |
Umfang: | print, 37 ref |
ISSN: | 0022-3263 (print) |
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