γ-Methyl-substituted-γ-butyrolactones: solid-phase synthesis employing a cyclisation–cleavage strategy
- 16 September 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (38) , 7293-7297
- https://doi.org/10.1016/s0040-4039(00)00921-7
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Solid-phase Synthesis, Antiviral Activity and Cytotoxicity of Some Functionalized LactonesPharmacy and Pharmacology Communications, 1999
- High Catalytic Activity of Chiral Amino Alcohol Ligands Anchored to Polystyrene ResinsThe Journal of Organic Chemistry, 1998
- Preparation of amides from acids and resin bound azides: Suppression of intramolecular lactam formationTetrahedron Letters, 1998
- Synthesis of (+)- and (−)-Phaseolinic Acid by Combination of Enzymatic Hydrolysis and Chemical Transformations with Revision of the Absolute Configuration of the Natural ProductThe Journal of Organic Chemistry, 1998
- Synthesis of functionalized γ-and δ-lactones via polymer-bound epoxidesTetrahedron Letters, 1997
- Lanthanide(III) trifluoromethanesulfonates as extraordinarily effective new catalysts for the aminolysis of 1,2-epoxidesTetrahedron Letters, 1994
- Synthesis of chiral functionalized trans-.beta.-isopropenyl-.gamma.-(hydroxymethyl)-.gamma.-butyrolactones.The Journal of Organic Chemistry, 1992
- Synthesis of optically active pheromonesTetrahedron, 1989
- 2-Siloxy-substituted methyl cyclopropanecarboxylates as building blocks in synthesis: efficient one-pot conversion to .gamma.-butyrolactonesThe Journal of Organic Chemistry, 1985
- Synthesis of Three Jasmin Constituents via a Central IntermediateHelvetica Chimica Acta, 1978