Synthesis of Substituted Se??Phenyl Selenocarboxylates from Terminal Alkynes

…, L Testaferri, A Temperini, L Bagnoli…

Index: Tiecco, Marcello; Testaferri, Lorenzo; Temperini, Andrea; Bagnoli, Luana; Marini, Francesca; Santi, Claudio; Terlizzi, Raffaella European Journal of Organic Chemistry, 2004 , # 16 p. 3447 - 3458

Full Text: HTML

Citation Number: 19

Abstract

Abstract Se-Phenyl selenocarboxylates have been conveniently prepared from (phenylseleno) acetylenes by treatment with p-toluenesulfonic acid monohydrate in dichloromethane. This easy conversion is compatible with a broad range of oxygen-and nitrogen-containing functional groups. The Se-phenyl selenocarboxylates were easily converted into the corresponding esters and amides.(© Wiley-VCH Verlag GmbH & Co. ...

Related Articles:

Total Synthesis of the Lycopodium Alkaloid Serratezomine A Using Free Radical-Mediated Vinyl Amination to Prepare a β-Stannyl Enamine Linchpin

[Pigza, Julie A.; Han, Jeong-Seok; Chandra, Aroop; Mutnick, Daniel; Pink, Maren; Johnston, Jeffrey N. Journal of Organic Chemistry, 2013 , vol. 78, # 3 p. 822 - 843]

Synthesis of thiazolo [4, 3-a] isoindoles by intramolecular cycloaddition-elimination reactions of 4-methyl-5-(substituted) imino-Δ 2-1, 2, 3, 4-thiatriazolines

[L'abbe, Gerrit; Leurs, Stefan; Sannen, Ingrid; Dehaen, Wim Tetrahedron, 1993 , vol. 49, # 20 p. 4439 - 4446]

Organolanthanide-catalyzed intramolecular hydroamination/cyclization of aminoalkynes

[Journal of the American Chemical Society, , vol. 118, # 39 p. 9295 - 9306]

Amino derivatives of indolone-N-oxide: Preparation and antiplasmodial properties

[European Journal of Medicinal Chemistry, , vol. 76, p. 369 - 375]

More Articles...