A novel Baylis–Hillman protocol for the synthesis of functionalized fused furans
- 5 February 2001
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 42 (6) , 1147-1149
- https://doi.org/10.1016/s0040-4039(00)02175-4
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Synthesis of stereochemically defined (E)-cinnamyl alcohol derivatives from the Baylis–Hillman adductsTetrahedron Letters, 2000
- Chiral Amine-Catalyzed Asymmetric Baylis−Hillman Reaction: A Reliable Route to Highly Enantiomerically Enriched (α-Methylene-β-hydroxy)estersJournal of the American Chemical Society, 1999
- Applications of the Baylis-Hillman Adducts in Organic Synthesis: A Facile Synthesis of [E]-α-Cyanocinnamyl Alcohols and [E]-α-Cyanocinnamic AldehydesSynlett, 1999
- A Facile One-Pot Conversion of Acetates of the Baylis−Hillman Adducts to [E]-α-Methylcinnamic AcidsThe Journal of Organic Chemistry, 1999
- Metal- and Ligand-Accelerated Catalysis of the Baylis−Hillman ReactionThe Journal of Organic Chemistry, 1998
- A one pot synthesis of (E)-4-alkylidene-2-cyclohexen-1-onesTetrahedron Letters, 1998
- A new protocol for the syntheses of (E)-3-benzylidenechroman-4-ones: a simple synthesis of the methyl ether of bonducellinChemical Communications, 1998
- The Friedel-Crafts reaction of the Baylis-Hillman adductsTetrahedron Letters, 1997
- The Baylis-Hillman reaction: A novel carbon-carbon bond forming reactionTetrahedron, 1996
- Synthetic potential of the tertiary-amine-catalysed reaction of activated vinyl carbanions with aldehydesTetrahedron, 1988