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Enantioselective One-Pot Rhodium-Catalyzed Cycloisomerization-Wittig Sequence to Chiral Functionalized 4-Alkyl 3-Alkylidene Tetrahydrofuran(on)es.
- Source :
-
Synlett . 2010, Issue 5, p782-786. 5p. - Publication Year :
- 2010
-
Abstract
- Alkyl and (hetero)aryl alkyne allyl alcohols can readily be transformed into chiral 4-alkyl 3-alkylidene tetrahydrofurans and tetrahydrofuranones bearing α,β-unsaturated carbonyl side chains in a one-pot fashion via an enantioselective rhodium-catalyzed �cycloisomerization-Wittig olefination sequence in good yields (54-86%). [ABSTRACT FROM AUTHOR]
- Subjects :
- *TETRAHYDROFURAN
*CYCLOISOMERIZATION
*ISOMERIZATION
*ALKYL compounds
*RHODIUM
Subjects
Details
- Language :
- English
- ISSN :
- 09365214
- Issue :
- 5
- Database :
- Academic Search Index
- Journal :
- Synlett
- Publication Type :
- Academic Journal
- Accession number :
- 95283503
- Full Text :
- https://doi.org/10.1055/s-0029-1219362