Synthesis of Substituted  Se ‐Phenyl Selenocarboxylates from Terminal Alkynes | Zendy

Tiecco Marcello | Zendy; Testaferri Lorenzo | Zendy; Temperini Andrea | Zendy; Bagnoli Luana | Zendy; Marini Francesca | Zendy; Santi Claudio | Zendy; Terlizzi Raffaella | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Synthesis of Substituted Se ‐Phenyl Selenocarboxylates from Terminal Alkynes

Author(s) -

Tiecco Marcello,

Testaferri Lorenzo,

Temperini Andrea,

Bagnoli Luana,

Marini Francesca,

Santi Claudio,

Terlizzi Raffaella

Publication year - 2004

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200400177

Subject(s) - chemistry , dichloromethane , nitrogen , alkyne , organic chemistry , medicinal chemistry , oxygen , catalysis , solvent

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. KGaA, 69451 Weinheim, Germany, 2004)

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research