A michael initiated - condensation - elimination sequence for the stereoselective synthesis of maleate derivatives.
- 1 January 1996
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 52 (4) , 1389-1398
- https://doi.org/10.1016/0040-4020(95)00965-5
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- 1,3-Dipolar Cycloadditions to Baylis-Hillman Adducts: Rationale for the Observed DiastereoselectivityThe Journal of Organic Chemistry, 1995
- Asymmetric Baylis-Hillman reactions using chiral 2,3-disubstituted 1,4-diazabicyclo[2.2.2]octanes catalysts under high pressure conditionsTetrahedron: Asymmetry, 1995
- Synthesis of ent-Cheilanthenediol, the Enantiomer of a Natural TricyclopentaprenediolSynlett, 1995
- Reaktionen von 4,4-Bis(trifluormethyl)-1,3-diazabuta-1,3-dienen. Synthese trifluormethyl-substituierter Heterocyclenvia Baylis-Hillman-ReaktionMonatshefte für Chemie / Chemical Monthly, 1995
- Baylis-Hillman Reaction: Magnesium Bromide as a Stereoselective Reagent for the Synthesis of [E]- and [Z]-Allyl BromidesSynlett, 1995
- Diethyl lithiomaleate: Preparation and use in synthesisTetrahedron Letters, 1994
- Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromaticsChemical Reviews, 1990
- Lithium diisopropylamide as a hydride donor. Reduction of aldehydes.Tetrahedron Letters, 1988
- New stereoselective synthesis of 20S and 20R steroidal side chains. Remarkable stereoselectivity differences between saturated and .alpha.,.beta.-unsaturated steroidal estersThe Journal of Organic Chemistry, 1988
- HYDROGEN TRANSFER OF 2,5-DIHYDROANISOLE TO HYDROGEN ACCEPTORS PROMOTED BY BUTYLLITHIUMChemistry Letters, 1982