Total Syntheses of Thiocoraline and BE-22179: Establishment of Relative and Absolute Stereochemistry
- 1 March 2000
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (12) , 2956-2957
- https://doi.org/10.1021/ja0001660
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- A Modified Friedlander Condensation for the Synthesis of 3-Hydroxyquinoline-2-carboxylatesThe Journal of Organic Chemistry, 1995
- Inhibition of Topoisomerase II by a Novel Antitumor Cyclic Depsipeptide, BE‐22179Japanese Journal of Cancer Research, 1994
- Non-Watson-Crick G ⋅ C and A ⋅ T Base Pairs in a DNA-Antibiotic ComplexScience, 1986
- The Synthesis of Cystine Peptides by Iodine Oxidation of S‐Trityl‐cysteine and S‐Acetamidomethyl‐cysteine PeptidesHelvetica Chimica Acta, 1980
- Efficient removal of N-benzyloxycarbonyl group by a ‘push–pull’ mechanism using thioanisole–trifluoroacetic acid, exemplified by a synthesis of Met-enkephalinJournal of the Chemical Society, Chemical Communications, 1980
- Structure revision of the antibiotic echinomycinJournal of the American Chemical Society, 1975
- Echinomycin: a bifunctional intercalating antibioticNature, 1974
- New synthesis of thiol estersThe Journal of Organic Chemistry, 1974
- Dimerization of an intermediate during the sodium in liquid ammonia reduction of l-thiazolidine-4-carboxylic acidCanadian Journal of Chemistry, 1967
- Stoffwechselprodukte von Actinomyceten. 15. Mitteilung. über die Konstitution von EchinomycinHelvetica Chimica Acta, 1959