Modular Approach toward the Construction of the Core Motifs of Annonaceous Acetogenins and Variants Thereof
- 7 February 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (5), 1368-1369
- https://doi.org/10.1021/jo972031r
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Parallel, Stereoselective Syntheses of both Enantiomers of Muricatacin and Their Sulfur and Nitrogen Relatives Using the Silyloxy Diene-Based MethodologyThe Journal of Organic Chemistry, 1997
- Expeditious Syntheses of Sugar-Modified Nucleosides and Collections Thereof Exploiting Furan-, Pyrrole-, and Thiophene-Based Siloxy DienesJournal of Medicinal Chemistry, 1997
- C-Clycosylation of cyclic N-acyliminium ions with trimethylsilyloxyfuranTetrahedron Letters, 1996
- A versatile synthesis of a β-turn peptidomimetic scaffold: An approach towards a designed model antagonist of the tachykinin NK-2 receptorBioorganic & Medicinal Chemistry Letters, 1996
- Recent advances in annonaceous acetogeninsNatural Product Reports, 1996
- Highly Efficient Synthesis of the Potent Antitumor Annonaceous Acetogenin (+)-ParviflorinJournal of the American Chemical Society, 1996
- Toward Chemical Libraries of Annonaceous Acetogenins. Total Synthesis of TrilobacinThe Journal of Organic Chemistry, 1996
- Stereoselective Approaches to Bioactive Carbohydrates and Alkaloids-With a Focus on Recent Syntheses Drawing from the Chiral PoolChemical Reviews, 1995
- Furan-, Pyrrole-, and Thiophene-Based Siloxydienes for Syntheses of Densely Functionalized Homochiral CompoundsSynthesis, 1995
- Design and synthesis of a prototypical non-peptidic inhibitor model for the enzme reninBioorganic & Medicinal Chemistry Letters, 1994