Total Synthesis of the Novel, Immunosuppressive Agent (−)-Pateamine A from Mycale sp. Employing a β-Lactam-Based Macrocyclization
- 1 January 1998
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (3), 591-592
- https://doi.org/10.1021/ja973549f
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Single-Step Synthesis of Cell-Permeable Protein Dimerizers That Activate Signal Transduction and Gene ExpressionJournal of the American Chemical Society, 1997
- A mild method for the alcoholysis of β-lactamsTetrahedron Letters, 1995
- Reductive Cleavage of TROC Groups Under Neutral Conditions with Cadmium-Lead CoupleTetrahedron Letters, 1995
- Structural and Synthetic Studies of the Pateamines: Synthesis and Absolute Configuration of the Hydroxydienoate FragmentTetrahedron Letters, 1995
- Catalytic, Asymmetric Synthesis of the Carbacephem FrameworkThe Journal of Organic Chemistry, 1994
- Asymmetric synthesis of (2R, 3S) and (2S, 3R) precursors of β-methyl-histidine, -phenylalanine and -tyrosineTetrahedron: Asymmetry, 1993
- Large rate accelerations in the stille reaction with tri-2-furylphosphine and triphenylarsine as palladium ligands: mechanistic and synthetic implicationsJournal of the American Chemical Society, 1991
- Pateamine: a potent cytotoxin from the New Zealand Marine sponge, mycale sp.Tetrahedron Letters, 1991
- Facile regioselective formation of thiopeptide linkages from oligopeptides with new thionation reagentsTetrahedron Letters, 1983
- Lysosomotropic Agents III1. Synthesis of N-Retinyl MorpholineSynthetic Communications, 1981