European Journal of Organic Chemistry · 2016 · 26 citations · 24 references
MedicineMedicinal ChemistryOncologyCancer PharmacologyDrug DiscoverySynthetic Medicinal ChemistryAntitumor AntibioticsOncology PharmacologyAnticancer ActivityMedicinal Chemistry ApplicationsPlant AlkaloidsSemisynthesis Of Natural Products
Ecteinascidin 743 is an antitumor drug used to treat specific soft‐tissue sarcomas (STS). In this paper, we present a concise and practical semisynthesis of ecteinascidin 743 starting from safracin B. The strategy involves the direct conversion of an aliphatic amino group into an acetoxy group. By this approach, ecteinascidin 743 was synthesized in 14 steps and 1.5 % overall yield. The synthetic approach also provided access to other tetrahydroisoquinoline alkaloids, such as (–)‐jorumycin (a promising anticancer candidate). (–)‐Jorumycin was prepared in six steps and 24.1 % overall yield from safracin B.
24
On the Mechanism of the Phenyl Isothiocyanate Degradation of Peptides.
Pehr Edman, Bengt Lindberg, H. I. Waterman et al. · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · 1956 · 321 citations · Full text
Total Synthesis of Ecteinascidin 743
Atsushi Endo, Arata Yanagisawa, Masanao Abe et al. · Journal of the American Chemical Society · 2002 · 288 citations