Short and efficient preparation of alkynyl selenides, sulfides and tellurides from terminal alkynes

Tetrahedron Letters

Volumn 45, Issue 13, 2004, Pages 2735-2737

  Bieber, Lothar W ^a   Da Silva, Margarete F ^a   Menezes, Paulo H ^a  

^a FEDERAL UNIVERSITY OF PERNAMBUCO   (Brazil)

Author keywords

Alkynyl selenides; Alkynyl sulfides; Alkynyl tellurides

Indexed keywords

ALKENYL GROUP; ALKYNE DERIVATIVE; ALKYNYL GROUP; BASE; COPPER DERIVATIVE; COPPER IODIDE; OXIDIZING AGENT; PHENYL GROUP; SELENIDE; SULFIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; ROOM TEMPERATURE;

EID: 1542328785     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.02.042     Document Type: Article

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29. General experimental procedure: A mixture of 0.25 mmol of the alkyne, 0.125 mmol of diphenyl dichalcogenide, 0.01 mmol of CuI and 0.5 mmol of base (where indicated) in 1.0 ml of commercial, undried DMSO was stirred at room temperature for the indicated time. After aqueous acidic work up and extraction with ether or dichloromethane, the crude products were purified by crystallization or distillation.