Design and synthesis of curacin a analogs with varied side chain structures

Design and synthesis of curacin a analogs with varied side chain structures Structure of Curacin A, a Novel Antimitotic, Antiproliferative and Brine Shrimp Toxic Natural Product from the Marine Cyanobacterium Lyngbya majuscula Curacin E from the Brittle Star Ophiocoma scolopendrina Biologically active taxol analogs with deleted A-ring side chain substituents and variable C-2' configurations Synthesis and Biological Evaluation of Structurally Highly Modified Analogues of the Antimitotic Natural Product Curacin A Curacins B and C, New Antimitotic Natural Products from the Marine Cyanobacterium Lyngbya majuscula Curacins B and C, New Antimitotic Natural Products from the Marine Cyanobacterium Lyngbya majuscula Curacin D, aN antimitotic agent from the marine Cyanobacterium Lyngbya majuscula Antitumor agents. 139. Synthesis and biological evaluation of thiocolchicine analogs 5,6-dihydro-6(S)-acyloxy)- and 5,6-dihydro-6(S)-[(aroyloxy)methyl]-1,2,3-trimethoxy-9-(methylthio)-8H-cyclohepta[a]naphthalen-8-ones as novel cytotoxic and antimitotic agents Relationships between the structure of taxol analogs and their antimitotic activity