Approaches to the Synthesis of Some Tyrosine-Derived Marine Sponge Metabolites: Synthesis of Verongamine and Purealidin N
| Autor: | Christopher D. Spilling, J. Jonathan Harburn, Todd R. Boehlow |
|---|---|
| Rok vydání: | 2001 |
| Předmět: |
Magnetic Resonance Spectroscopy
Chemistry Decarboxylation Metabolite Organic Chemistry Histamine Antagonists Halogenation Antineoplastic Agents Spectrometry Mass Fast Atom Bombardment Nitro Compounds Oxime Phosphonate Porifera chemistry.chemical_compound Hydrolysis Oximes Acetone Animals Receptors Histamine H3 Tyrosine Organic chemistry Dimethyldioxirane Oxidation-Reduction Bromobenzenes |
| Zdroj: | The Journal of Organic Chemistry. 66:3111-3118 |
| ISSN: | 1520-6904 0022-3263 |
| Popis: | The oxidation of tyrosine ethyl ester (7) with Na(2)WO(4)/H(2)O(2) in ethanol, dimethyldioxirane in acetone, or methyltrioxorhenium/H(2)O(2) in EtOH gave the corresponding tyrosine oxime (8) in high yield. Controlled bromination of the aromatic ring gave the monobromo oxime (9), the dibromo oxime (10), or the spiroisoxazoline (11) depending upon reaction conditions. Synthesis of the known metabolite verongamine (15) was achieved by oxidation of O-methyl bromotyrosine methyl ester and amidation of the resulting oxime ester (14) with histamine. The mono- and di-bromotyrosine oxime derivatives (9 and 10) were further transformed into the naturally occurring nitriles (16 and 17) by base hydrolysis of the ester and acid-catalyzed decarboxylation. Wadsworth-Emmons olefination of the dibromobenzaldehyde (20b) with phosphonate (18) gave the pyruvate silylenolether (21b). Deprotection and in situ oxime formation gave the oxime ester (23b). Attempted purification of the pyruvate ester resulted in a homoaldol condensation yielding butenolide (22). Amidation of the oxime ester (23b) with histamine, followed by deprotection of the MOM ether gave the first synthesis of purealidin N (28). Oxidative spirocyclization of the phenolic oxime ester (23d) with a polymer-bound iodosyl diacetate gave the spiroisoxazoline (24) and represents a formal synthesis of aerothionin (26a), homoaerothionin (26b), and aerophobin-1 (25). |
| Databáze: | OpenAIRE |
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