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Copper-catalyzed O-alkenylation of phosphonates
- Source :
- Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 611-615 (2020), Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela, instname
- Publication Year :
- 2020
- Publisher :
- Beilstein Institut, 2020.
-
Abstract
- Copper catalysis allows the direct oxygen alkenylation of dialkyl phosphonates with alkenyl(aryl)iodonium salts with selective transfer of the alkenyl group. This novel methodology proceeds with a wide range of phosphonates under mild conditions and gives straightforward access to valuable enol phosphonates in very good yields. Financial support from the AEI (CTQ2017-88451-R), Xunta de Galicia (ED431F 2016/006; ED431C 2018/04; Centro singular de investigación de Galicia accreditation 2016-2019, ED431G/09) and the European Union (ERDF) is gratefully acknowledged. N. V.-G. thanks AEI for a predoctoral FPI fellowship SI
- Subjects :
- Alkenylation
c(sp2)–o bond formation
Hypervalent Iodine
chemistry.chemical_element
C(sp2)–O Bond Formation
010402 general chemistry
01 natural sciences
Medicinal chemistry
Catalysis
lcsh:QD241-441
chemistry.chemical_compound
lcsh:Organic chemistry
Selective transfer
alkenylation
lcsh:Science
010405 organic chemistry
Aryl
Organic Chemistry
phosphonates
Enol
Copper
0104 chemical sciences
hypervalent iodine
chemistry
copper
Copper catalyzed
lcsh:Q
Phosphonates
Subjects
Details
- ISSN :
- 18605397
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Beilstein Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....b69b82f91e27efe6de08e762cac49a84