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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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Publisher copy:
10.1055/s-1997-705

Authors


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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


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

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