Synthesis of 5‐/10‐Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)‐Mediated Ring‐Closure Reaction
- 1 April 1996
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1996 (4) , 447-456
- https://doi.org/10.1002/jlac.199619960405
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Chemistry and Biology of the Enediyne Anticancer AntibioticsAngewandte Chemie International Edition in English, 1991
- Chemie und Biologie von Endiin‐Cytostatica/AntibioticaAngewandte Chemie, 1991
- General methodology for the synthesis of neocarzinostatin chromophore analogs: intramolecular chromium-mediated closures for strained ring synthesisJournal of the American Chemical Society, 1990
- Synthesis of a new 10-membered ring functionalised cyclodiynol related to neocarziostatin chromophoreTetrahedron Letters, 1990
- A new route to 10-membered ring analogues of neocarzinostatin chromophoreTetrahedron Letters, 1990
- The 10-membered ring analogs of neocarzinostatin chromophore: design, synthesis and mode of decompositionJournal of the American Chemical Society, 1989
- Mechanism of activation of the antitumor antibiotic neocarzinostatin by mercaptan and sodium borohydride.The Journal of Antibiotics, 1989
- Studies on DNA - active agents: The synthesis of the parent carbocyclic subunit of neocarzinostatin chromophore ATetrahedron Letters, 1988
- Proposed structure of the neocarzinostatin chromophore-methyl thioglycolate adduct; A mechanism for the nucleophilic activation of neocarzinostatinTetrahedron Letters, 1987
- The structure of neocarzinostatin chromophore possessing a novel bicyclo-[7,3,0]dodecadiyne systemTetrahedron Letters, 1985