Synthesen von 2,3-Dioxoalkylphosphonaten und anderer neuartiger ?-Ketophosphonate sowie eines Phosphinopyruvamids ( = (Alkyloxyphosphinyl)pyruvamids)

Autor: Helmut Feistauer, Richard Neidlein
Rok vydání: 1996
Předmět:
Zdroj: Helvetica Chimica Acta. 79:895-912
ISSN: 1522-2675
0018-019X
DOI: 10.1002/hlca.19960790329
Popis: Syntheses of 2,3-Dioxoalkylphonates and Other Novel β-Ketophosphonates As Well As of a Phosphinopyruvamide ( = (Alkyloxyphosphinyl)pyruvamide) The new 3-(diethoxyphosphoryl)-2-oxopropanoates 5 and 6 and -propanamides 1–4 with various amino substituents at C(3) were prepared (Scheme 2). These compounds exist, depending on N-substitution, as pure (E)-enols (in the case of1 and 5) or as a mixture of three tautomeric forms (in the case of 1–4 and 6). The configuration could be unambiguously assigned from the 1H-, 13C-, and 31P-NMR spectra. Phosphinopyruvamide ( = (alkyloxyphosphinyl)pyruvamide) 9 was prepared in a similar manner in spite of the instability of phosphinate derived carbanions. Some 3-(ethoxyimino)-2-oxobutylphosphonates, 11–13 (Scheme 5), and various 3,3-dimethoxy-2-oxoalkylphosphonates, 19–23 and 26–33 (Scheme 6), were available from the reaction of lithioalkylphosphonates with 2-(ethoxyimino)propanoates and 2,2-dimethoxyalkanoates, respectively. The 3,3-dimethoxybutylphosphonates 20, and 26–30 were cleaved to give 2,3-dioxobutylphosphonates 34–39 (Scheme 6). This method provides easy access to a new class of potentially pharmaceutically useful compounds.
Databáze: OpenAIRE
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