Indole arylation studies directed towards the synthesis of simplified eastern subunits of chloropeptin and kistamycin
- 18 June 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (25) , 4467-4470
- https://doi.org/10.1016/s0040-4039(98)00818-1
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- The first synthesis of 16+15-membered bicyclic polypeptide model of A-O-C-B-O-D rings of kistamicinTetrahedron Letters, 1997
- Synthesis of a model of chloropeptins I, II western subunit by the intramolecular SNAr based methodologyTetrahedron Letters, 1997
- The first synthesis of a 15-membered macrocycle. Model of ring I of kistamycinTetrahedron Letters, 1997
- Synthesis of CC biaryl segment of complestatin and chloropeptin: Approach to the right hand CEF-ring system of complestatinTetrahedron Letters, 1997
- Stereostructure of (−)-Chloropeptin I, a Novel Inhibitor of gp120−CD4 Binding, via High- Temperature Molecular Dynamics, Monte Carlo Conformational Searching, and NMR SpectroscopyJournal of the American Chemical Society, 1996
- Chloropeptins I and II, novel inhibitors against gp120-CD4 binding from Streptomyces sp.The Journal of Antibiotics, 1994
- Synthesis of 6- and 7-ArylindolesviaPalladium-Catalyzed Cross-Coupling of 6- and 7-Bromoindole with Arylboronic AcidsSynlett, 1994
- New antiviral antibiotics, Kistamicins A and B. II. Structure determination.The Journal of Antibiotics, 1993
- New antiviral antibiotics, Kistamicins A and B. I. Taxonomy, production, isolation, physico-chemical properties and biological activities.The Journal of Antibiotics, 1993
- Synthesis of Some 5-Substituted IndolesHETEROCYCLES, 1992