Title of article :
Acceleration effect of allylic hydroxy group on ring-closing enyne metathesis of terminal alkynes: scope and application to the synthesis of isofagomine
Author/Authors :
Imahori، نويسنده , , Tatsushi and Ojima، نويسنده , , Hidetomo and Tateyama، نويسنده , , Hiroki and Mihara، نويسنده , , Yukiko and Takahata، نويسنده , , Hiroki، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2008
Pages :
4
From page :
265
To page :
268
Abstract :
An interesting allylic substituent effect on ring-closing enyne metathesis has been found. An allylic hydroxy group on enyne substrates accelerates ring-closing enyne metathesis of terminal alkynes. The reaction proceeds smoothly without ethylene atmosphere and/or more reactive newer generation Ru-carbene catalysts, which are generally necessary to promote the reaction. This efficient reaction was applied to the synthesis of isofagomine.
Journal title :
Tetrahedron Letters
Serial Year :
2008
Journal title :
Tetrahedron Letters
Record number :
1859963
Link To Document :
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