Fragmentation-Related Phosphonylation of Nucleophiles Utilizing P-Alkyl 2,3-oxaphosphabicyclo[2.2.2]octene 3-oxide Precursors

Tamara Kovács, Laura Szandra Fülöp, G. Keglevich

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

New P-alkyl 2,3-oxaphosphabicyclo-[2.2.2]octene 3-oxides were synthesized by the Bayer-Villiger oxidation of the corresponding 7-phosphanorbornene 7-oxides and were used as precursors for reactive alkylmetaphosphonates useful in the phosphonylation of alcohols. This is the first case that the reactivity of the two regioisomers formed by O-insertion was differentiated and that the fragmentation-related phosphonylation leading to phosphonic acid-esters was achieved under microwave-assisted conditions.

Original languageEnglish
Pages (from-to)83-90
Number of pages8
JournalHeteroatom Chemistry
Volume27
Issue number2
DOIs
Publication statusPublished - Mar 1 2016

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Nucleophiles
Oxides
Organophosphonates
Microwaves
Alcohols
Oxidation

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Fragmentation-Related Phosphonylation of Nucleophiles Utilizing P-Alkyl 2,3-oxaphosphabicyclo[2.2.2]octene 3-oxide Precursors. / Kovács, Tamara; Fülöp, Laura Szandra; Keglevich, G.

In: Heteroatom Chemistry, Vol. 27, No. 2, 01.03.2016, p. 83-90.

Research output: Contribution to journalArticle

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