Optically Active Allenes from β-Lactone Templates: Asymmetric Total Synthesis of (−)-Malyngolide
- 1 October 2000
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (42) , 10470-10471
- https://doi.org/10.1021/ja002783u
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Catalytic Asymmetric Propionate Aldol Reactions via Acyl Halide−Aldehyde CyclocondensationsOrganic Letters, 2000
- Catalytic Asymmetric Acyl Halide−Aldehyde Cyclocondensations. A Strategy for Enantioselective Catalyzed Cross Aldol ReactionsJournal of the American Chemical Society, 1999
- Mechanistic aspects of the formation of chiral allenes from propargylic ethers and organocopper reagentsJournal of the American Chemical Society, 1990
- Synthesis and stereochemistry of allenes. Part 3. Highly stereoselective synthesis of chiral alkyl allenes by organocopper(I)-induced anti 1,3-substitution of chiral propynyl estersThe Journal of Organic Chemistry, 1989
- Are allenes formed from propargylic ethers through aTetrahedron Letters, 1986
- Cyclisation d'oximes β-alleniques. Synthese de dihydro-4,7 oxazepines-1,2Tetrahedron Letters, 1985
- Acylation-cycloalkylation. A new annelation route to eudesmanesThe Journal of Organic Chemistry, 1979
- Allenes and acetylenes. 22. Mechanistic aspects of the allene-forming reductions (SN2' reaction) of chiral propargylic derivatives with hydride reagentsJournal of the American Chemical Society, 1979
- Allenes and Acetylenes. XXI. Leaving-group Effects on the Stereochemistry of Allene-forming Organocuprate Reactions.Acta Chemica Scandinavica, 1979
- Novel synthesis of substituted allenesJournal of the American Chemical Society, 1969