Iodosobenzene tetrafluoroborate: First example of a stable electrophilic hypervalent iodine reagent without nucleophilic ligands

Autor:	Viktor V. Zhdankin, B. Berglund, Rik R. Tykwinski, Ronald Caple, Nikolai S. Zefirov, Anatoly S. Koz'min
Rok vydání:	1988
Předmět:	Iodosobenzene chemistry.chemical_classification Tetrafluoroborate Silylation Chemistry Organic Chemistry Hypervalent molecule Biochemistry Enol Medicinal chemistry chemistry.chemical_compound Nucleophile Drug Discovery Electrophile Enol ether Organic chemistry
Zdroj:	Tetrahedron Letters. 29:3717-3720
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(00)82162-0
Popis:	Iodosobenzene tetrafluoroborate 1 ha been prepared by the reaction of PhI(OAc) 2 and aquenous HBF 4 , and its reactions with alkenes, silyl enol ethers, and acetylenes have been studied.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::3cce1d57e0a54e09944932bcfa9a3ba7 https://doi.org/10.1016/s0040-4039(00)82162-0 Zobrazit plný text záznamu