Studies on the synthesis of the antitumor agent CC-1065. Synthesis of PDE I and PDE II, inhibitors of cyclic adenosine-3',5'-monophosphate phosphodiesterase using the 3,3'-bipyrrole strategy
- 1 April 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 109 (9), 2711-2717
- https://doi.org/10.1021/ja00243a026
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Studies on the synthesis of the antitumor agent CC-1065. Synthesis of the unprotected cyclopropapyrroloindole A portion using the 3,3'-bipyrrole strategyJournal of the American Chemical Society, 1987
- Reaction of the Antitumor Antibiotic CC-1065 with DNA: Structure of a DNA Adduct with DNA Sequence SpecificityScience, 1984
- Intramolecular Diels-Alder reactions of 1,2-diazines: general indoline synthesis. Studies on the preparation of the central and right-hand segments of CC-1065The Journal of Organic Chemistry, 1984
- Biosynthesis of the antitumor antibiotic CC-1065 by Streptomyces zelensis.The Journal of Antibiotics, 1983
- Total Synthesis of PDE-IIAgricultural and Biological Chemistry, 1979
- Total Synthesis of PDE-IAgricultural and Biological Chemistry, 1979
- Isolation and Characterization of PDE-I and II, the Inhibitors of Cyclic Adenosine-3′,5′-monophosphate PhosphodiesteraseAgricultural and Biological Chemistry, 1978
- Deuterium or tritium labeling by ionic hydrogenation. A convenient route to specifically labeled dethiobiotinThe Journal of Organic Chemistry, 1977
- Reaction of O-methyl-N,N'-diisopropylisourea with amino acids and aminesThe Journal of Organic Chemistry, 1977
- 95. Zwei Synthesen des α-Melanotropins (α-MSH) mit Hilfe leicht entfernbarer Schutzgruppen)Helvetica Chimica Acta, 1963