- Abstract:
- A systematically varied series of conformationally restricted ketones, readily prepared from N-acetyl-D-glucosamine, were tested against representative olefins as asymmetric epoxidation catalysts showing useful selectivities against terminal olefins and, in particular, typically difficult 2,2-disubstituted terminal olefins.
- Publication status:
- Published
- Publisher copy:
- 10.1039/b911675c
-
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- Journal:
- Organic and biomolecular chemistry
- Volume:
- 7
- Issue:
- 20
- Pages:
- 4285-4288
- Publication date:
- 2009-10-05
- DOI:
- EISSN:
-
1477-0539
- ISSN:
-
1477-0520
- URN:
-
uuid:87b1300a-7790-4685-94ee-a38bf4855888
- Source identifiers:
-
34912
- Local pid:
- pubs:34912
- Language:
- English
- Keywords:
- Copyright date:
- 2009
Journal article
Accessible sugars as asymmetric olefin epoxidation organocatalysts: glucosaminide ketones in the synthesis of terminal epoxides.
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