Journal article
Stereoselective methodology for 1-aryl-1-alkyl epoxides via chromium tricarbonyl complexes
- Abstract:
- Treatment of (1RS, SSR)-(1-phenylsulfinyl-2-valeryl benzene) chromium tricarbonyl 2 with a sulfur ylide results in a highly diastereoselective epoxide formation (d.s.>96:4). Regioselective opening of the epoxide, employing an in situ trapping protocol, allows the synthesis of a highly functionalised, diastereomerically pure benzylic alcohol.
- Publication status:
- Published
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Authors
- Journal:
- SYNLETT More from this journal
- Volume:
- 1997
- Issue:
- 1
- Pages:
- 66-and
- Publication date:
- 1997-01-01
- DOI:
- EISSN:
-
1437-2096
- ISSN:
-
0936-5214
- Keywords:
- Pubs id:
-
pubs:110835
- UUID:
-
uuid:3c38c3eb-c4f3-4244-97a1-79c2ac61b825
- Local pid:
-
pubs:110835
- Source identifiers:
-
110835
- Deposit date:
-
2012-12-19
Terms of use
- Copyright date:
- 1997
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