Acid-promoted transformations of aryl substituted diphenylphosphoryl allenes

Autor:	Albina V. Dogadina, Aleksander V. Vasilyev, Stanislav V. Lozovskiy, Alexander S. Bogachenkov
Rok vydání:	2016
Předmět:	chemistry.chemical_compound 010405 organic chemistry Chemistry Allene Aryl Organic Chemistry Drug Discovery Organic chemistry 010402 general chemistry 01 natural sciences Biochemistry 0104 chemical sciences
Zdroj:	Tetrahedron Letters. 57:3167-3170
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2016.06.026
Popis:	1-(Diphenylphosphoryl)alka-1,2-dienes, bearing aryl substituents at the allene system, under the action of Bronsted (TfOH, H2SO4) or Lewis (AlCl3) acids gave rise to 3-hydroxyalk-2-en-1-yl-diphenylphosphine oxides (diphenylphosphoryl allyl alcohols) in yields of 57–98%. In some cases, the formation of (diphenylphosphoryl)indenes and phosphaheterobicyclic structures was observed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d94bdc02f3558a421e94ae92ba0f2468 https://doi.org/10.1016/j.tetlet.2016.06.026 Zobrazit plný text záznamu Full Text from ScienceDirect