Design and synthesis of curacin a analogs with varied side chain structures
- 21 October 1997
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 7 (20) , 2657-2660
- https://doi.org/10.1016/s0960-894x(97)10055-5
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- A mild and selective deprotection of p-methoxybenzyl (PMB) ether by magnesium bromide diethyl etherate-methyl sulfideTetrahedron Letters, 1997
- Synthetic study on curacin A: A novel antimitotic agent from the cyanobacterium Lyngbya majusculaTetrahedron, 1996
- Efficient asymmetric synthesis of cis-2-methylcyclopropanecarboxylic acidTetrahedron, 1996
- Asymmetric total synthesis of curacin ATetrahedron Letters, 1996
- Synthetic study of curacin A: Synthesis of partial structure of curacin A and elucidation of the absolute stereochemistry at the methylcyclopropylthiazoline moietyTetrahedron Letters, 1995
- Structure of Curacin A, a Novel Antimitotic, Antiproliferative and Brine Shrimp Toxic Natural Product from the Marine Cyanobacterium Lyngbya majusculaThe Journal of Organic Chemistry, 1994
- Antimitotic agents: Chemistry and recognition of tubulin moleculeMedicinal Research Reviews, 1993
- Studies on macrocyclic lactone antibiotics. XI. Anti-mitotic and anti-tubulin activity of new antitumor antibiotics, rhizoxin and its homologues.The Journal of Antibiotics, 1987