Stereoselective Synthesis of Functionalized Carbocycles and Heterocycles via an Ester Enolate Claisen/Ring-Closing Metathesis Manifold,
- 22 April 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (10) , 3158-3159
- https://doi.org/10.1021/jo980118m
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Synthesis and Applications of RuCl2(CHR‘)(PR3)2: The Influence of the Alkylidene Moiety on Metathesis ActivityJournal of the American Chemical Society, 1996
- Ring-Closing Metathesis and Related Processes in Organic SynthesisAccounts of Chemical Research, 1995
- Synthesis of Chiral γ,δ‐Unsaturated Amino Acids by Asymmetric Ester Enolate Claisen RearrangementAngewandte Chemie International Edition in English, 1995
- Synthesis of Unsaturated Amino Acids by [3,3]‐Sigmatropic Rearrangement of Chelate‐Bridged Glycine Ester EnolatesAngewandte Chemie International Edition in English, 1994
- Reaction of aminopropanedinitrile 4-methylbenzenesulfonate [aminomalononitrile p-toluenesulfonate (tosylate)] with aromatic aldehydesThe Journal of Organic Chemistry, 1991
- Fluorine-19 NMR study on the conformation changes of 1,1,2,2-tetrafluoro-1,2-disilacyclohexanesThe Journal of Organic Chemistry, 1983
- Enolate claisen rearrangement of glycolate estersTetrahedron Letters, 1983
- Ester-enolate Claisen rearrangement of lactic acid derivativesThe Journal of Organic Chemistry, 1982
- Control of remote relative chiralities: a stereospecific total synthesis of dl-widdrolJournal of the American Chemical Society, 1980
- Ozonolysis of trans-2,3-dichloro-2-butene. Isolation of .alpha.-chloro peroxidesJournal of the American Chemical Society, 1976