Preparation and rearrangement of 2-allyloxyethyl aryl sulfoxides; a mercury-free claisen sequence
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (28) , 4041-4044
- https://doi.org/10.1016/s0040-4039(00)94494-0
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- The thermal, aliphatic Claisen rearrangementChemical Reviews, 1988
- Modeling chemical reactivity. 3. Stereochemistry of Michael additions of vinyl sulfoxidesJournal of the American Chemical Society, 1986
- Intramolecular michael addition reaction to chiral vinylic sulfoxides. An enantioselective synthesis of (R)- and (S)-1,7-dioxaspiro[5.5]undecaneTetrahedron Letters, 1985
- A new and facile route to spiro-ketal skeleton highly stereoselective CO bond formation by intramolecular Michael addition to δ,β-unsaturated sulfoxidesTetrahedron Letters, 1984
- Application of chiral sulfoxides in asymmetric synthesis: the enantiospecific synthesis of the chroman ring of .alpha.-tocopherol (vitamin E)Journal of the American Chemical Society, 1984
- Preparation and rearrangement of trans-3-(allyloxy)acrylic acids: a Claisen sequence that avoids mercury catalysisThe Journal of Organic Chemistry, 1983
- SYNTHETIC UTILITY OF A FLUORINE-FACILITATED CLAISEN REARRANGEMENT: A NOVEL SYNTHETIC METHOD FOR 2,4-ALKADIENOIC ACIDS USING 2,2,2-TRIFLUOROETHYL PHENYL SULFOXIDEChemistry Letters, 1981