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pro vyhledávání: '"Perkow reaction"'
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Publikováno v:
Russian Journal of General Chemistry. 90:89-92
Addition of ethanol and diethyl phosphonate to the carbonyl group of 2,2-dichloro-2-(diethoxyphosphoryl)-acetaldehyde has been studied, and the corresponding α-chloro ether, acetal, and phosphorylated metrifonate have been obtained. α,α-Dichloro-
Autor:
Enxue Shi, Zhenhua Gao, Yongbiao Guo, Junchen Li, Chengxin Pei, Yuepeng Cao, Xiaojing Bi, Ling Yuan
Publikováno v:
RSC Advances. 10:29493-29497
A regioselective O/C phosphorylation of α-chloroketones with trialkyl phosphites was performed for the first time, which employed solvent-free Perkow reaction and NaI-assisted Arbuzov reaction under mild conditions respectively. Versatile enol phosp
Publikováno v:
Molecules
Volume 25
Issue 10
Molecules, Vol 25, Iss 2430, p 2430 (2020)
Volume 25
Issue 10
Molecules, Vol 25, Iss 2430, p 2430 (2020)
Organophosphorus compounds occupy a significant position among the plethora of organic compounds, but a limited number of paramagnetic phosphorus compounds have been reported, including paramagnetic phosphonates. This paper describes the syntheses an
Autor:
Tomáš Tobrman, Peter Polák
Publikováno v:
Organic & Biomolecular Chemistry. 15:6233-6241
A novel methodology for the synthesis of functionalised indoles based on the cross-coupling reactions of 3-bromo-2-indolyl phosphates is described. The preparation involves the conversion of easily available 2-oxindoles to 3,3-dibromo-2-oxindoles fol
Publikováno v:
Organicbiomolecular chemistry. 16(32)
An inorganic base-promoted domino reaction with organophosphites and acyl cyclopropane derivatives is developed and proved to provide an efficient access to functionalized enol phosphates. Unlike the well-known Perkow reaction, which employs trialkyl
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2017, 28 (19), pp.2637-2641. ⟨10.1055/s-0036-1590856⟩
SYNLETT, Georg Thieme Verlag, 2017, 28 (19), pp.2637-2641. ⟨10.1055/s-0036-1590856⟩
A one-pot, four-component synthesis of imido phosphates has been achieved using a Nef–Perkow sequence followed by addition of carboxylic acid derivatives. The final imido moiety is formed via a Mumm rearrangement of an intermediate imidate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fc122be875dbd2f5410168827b7c97c
https://hal.archives-ouvertes.fr/hal-01664663
https://hal.archives-ouvertes.fr/hal-01664663
Autor:
Arturo Espinosa Ferao
Publikováno v:
The journal of physical chemistry. A. 121(34)
Two competitive mechanistic pathways for the reaction between trimethyl phosphite and chloroacetone are analyzed by high-level calculations. FMO analysis and HSAB-derived descriptors point to a preferential initial interaction of the nucleophile with
Autor:
G. A. Ivkova, Rashid Z. Musin, Ekaterina V. Mironova, Dmitry B. Krivolapov, Aidar T. Gubaidullin, L. M. Abdrakhmanova, Vladimir F. Mironov
The interaction of 2-(5-methyl-2-phenyl-2H-1,2,3-diazaphosphol-4-yl)-4H-benzo[e]-1,3,2-dioxaphosphinin-4-one with mesoxalic and trifluoropyruvic acids ethyl and diethyl esters, hexafluoroacetone and chloral proceeds with an exclusive participation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a371bf1c632f5c6ff65dcc13671f075f
Publikováno v:
Helvetica Chimica Acta. 97:1004-1008
Imidoyl chlorides, generated from isocyanides and acyl chlorides, react with trialkyl phosphites, in a Perkow-type reaction, to afford 3-(alkylimino)-2-[(dialkyloxyphosphoryl)oxy]acrylates, which undergo a smooth reaction with tosylmethyl isocyanide