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Methyl 4-toluenesulfonyloxymethylphosphonate, a new and versatile reagent for the convenient synthesis of phosphonate-containing compounds

SYSNO ASEP	0332679
Document Type	J - Journal Article
R&D Document Type	Journal Article
Subsidiary J	Článek ve WOS
Title	Methyl 4-toluenesulfonyloxymethylphosphonate, a new and versatile reagent for the convenient synthesis of phosphonate-containing compounds
Author(s)	Markusová Kóšiová, Ivana (UOCHB-X)_{RID, ORCID} Točík, Zdeněk (UOCHB-X) Buděšínský, Miloš (UOCHB-X)_{RID, ORCID} Šimák, Ondřej (UOCHB-X)_RID Liboska, Radek (UOCHB-X)_{RID, ORCID} Rejman, Dominik (UOCHB-X)_{RID, ORCID} Pačes, Ondřej (UOCHB-X) Rosenberg, Ivan (UOCHB-X)_{RID, ORCID}
Number of authors	8
Source Title	Tetrahedron Letters. - : Elsevier - ISSN 0040-4039 Roč. 50, č. 49 (2009), s. 6745-6747
Number of pages	3 s.
Language	eng - English
Country	GB - United Kingdom
Keywords	nucleoside phosphonates ; phosphonylation ; methyl 4-toluenesulfonyloxymethylphosphonate
Subject RIV	CC - Organic Chemistry
R&D Projects	GA202/09/0193 GA ČR - Czech Science Foundation (CSF)
	GA203/09/0820 GA ČR - Czech Science Foundation (CSF)
	LC06061 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
	LC06077 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
	KAN200520801 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
CEZ	AV0Z40550506 - UOCHB-X (2005-2011)
UT WOS	000271603000002
DOI	10.1016/j.tetlet.2009.09.062
Annotation	A convenient procedure leading to new phosphonylating reagent, requiring no chromatographic purification, is described. This stable reagent is efficient in phosphonylations and causes no unwanted methylation in nucleoside molecule.
Workplace	Institute of Organic Chemistry and Biochemistry
Contact	asep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434
Year of Publishing	2010

Number of the records: 1