1038749-06-2Relevant academic research and scientific papers
Gold-catalyzed cyclization of enyne-1,6-diols to substituted furans
Kim, Sundae,Kang, Dongjin,Shin, Seunghoon,Lee, Phil Ho
scheme or table, p. 1899 - 1901 (2010/09/07)
Treatment of enyne-1,6-diols with 5 mol % Ph3PAuCl in the presence of 5 mol % AgOTf as a cocatalyst selectively produced trisubstituted furans in good to excellent yields in dichloromethane at room temperature for 5-10 min through cyclization f
Regioselective addition of allylindium reagents to allenes in functionalized 1,6-diols bearing allenynes
Kim, Sundae,Lee, Phil Ho
supporting information; experimental part, p. 2262 - 2266 (2009/04/07)
Addition reactions of allylindium reagents generated in situ from indium and allyl halides to functionalized allenyne 1,6-diols proceeded regioselectively through anti-Markovnikov addition to produce exclusively dienyne 1,6-diols in good yields in THF at
Highly selective synthetic method for 1,6-diols bearing enyne functions: Development of 3,6-dianion reagent of 1,2-hexadien-4-yne using 1,6-dibromo-2,4-hexadiyne and indium
Kim, Sundae,Lee, Kooyeon,Seomoon, Dong,Lee, Phil Ho
, p. 2449 - 2453 (2008/09/19)
The reaction of aldehydes and ketones with an organoindium reagent generated in situ from indium and 2,6-dibromo-2,4-hexadiyne in the presence of lithium iodide in tetrahydrofuran (THF) selectively produced 1,6-diols linked to an allenyne unit with comple
