Convergent Synthesis of Dolastatin 15 by Solid Phase Coupling of anN-Methylamino Acid
- 1 January 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (2) , 405-411
- https://doi.org/10.1021/jo981055a
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Convergent Synthesis of (−)-Mirabazole C Using a Chloroimidazolidium Coupling Reagent, CIPThe Journal of Organic Chemistry, 1996
- Coupling N-Methylated Amino Acids Using PyBroP and PyCloP Halogenophosphonium Salts: Mechanism and Fields of ApplicationThe Journal of Organic Chemistry, 1994
- Advantageous applications of azabenzotriazole (triazolopyridine)-based coupling reagents to solid-phase peptide synthesisJournal of the Chemical Society, Chemical Communications, 1994
- 1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additiveJournal of the American Chemical Society, 1993
- Antineoplastic agents. 220. Synthesis of natural (-)-dolastatin 15Journal of the American Chemical Society, 1991
- 2‐Chlorotrityl chloride resinInternational Journal of Peptide and Protein Research, 1991
- Isolation and structure of the cytostatic linear depsipeptide dolastatin 15The Journal of Organic Chemistry, 1989
- New methods and reagents in organic synthesis. 14. A simple efficient preparation of methyl esters with trimethylsilyldiazomethane (TMSCHN2) and its application to gas chromatographic analysis of fatty acids.CHEMICAL & PHARMACEUTICAL BULLETIN, 1981
- Protection of hydroxyl groups as tert-butyldimethylsilyl derivativesJournal of the American Chemical Society, 1972
- 272. N-substituted amino-acids. Part I. A new method of preparation of dimethylamino-acidsJournal of the Chemical Society, 1950