Synthesis of the orienticin C M(2–4) macrocycle utilizing a nucleophilic aromatic substitution strategy
- 1 May 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (19) , 3251-3254
- https://doi.org/10.1016/0040-4039(96)00582-5
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Synthesis of appropriately functionalized vancomycin CD and DE ring systemsBioorganic & Medicinal Chemistry Letters, 1995
- Studies directed toward the synthesis of vancomycin and related cyclic peptidesChemical Reviews, 1995
- Synthesis of A Modified Carboxylate-binding Pocket of VancomycinTetrahedron Letters, 1995
- SNAr-Based Macrocyclization: An Application to the Synthesis of Vancomycin Family ModelsThe Journal of Organic Chemistry, 1994
- The first examples of SNAr-based macrocyclisation: synthesis of model carboxylate-binding pockets of vancomycinJournal of the Chemical Society, Chemical Communications, 1994
- The asymmetric synthesis of .alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-.alpha.-azido carboxylic acidsJournal of the American Chemical Society, 1990
- The oxidative macrocyclization of phenolic peptides. A biomimetic approach to the synthesis of the vancomycin family of antibioticsJournal of the American Chemical Society, 1989
- Synthesis of the cyclic hexapeptide echinocandin D. New approaches to the asymmetric synthesis of .beta.-hydroxy .alpha.-amino acidsJournal of the American Chemical Society, 1987
- THE STRUCTURE AND MODE OF ACTION OF GLYCOPEPTIDE ANTIBIOTICS OF THE VANCOMYCIN GROUPAnnual Review of Microbiology, 1984
- Alkyl nitrite-metal halide deamination reactions. 6. Direct synthesis of arenediazonium tetrafluoroborate salts from aromatic amines, tert-butyl nitrite, and boron trifluoride etherate in anhydrous mediaThe Journal of Organic Chemistry, 1979