Title of article :
Ring-closing metathesis as a new methodology for the synthesis of monomeric flavonoids and neoflavonoids
Author/Authors :
Miller، نويسنده , , Bradley J. and Pieterse، نويسنده , , Tanya and Marais، نويسنده , , Charlene and Bezuidenhoudt، نويسنده , , Barend C.B.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2012
Pages :
3
From page :
4708
To page :
4710
Abstract :
Basic flavonoid (flavene) and neoflavonoid (neoflavene) skeletons were successfully synthesized using ring-closing metathesis, showing that this methodology can be used as a central synthetic tool for the synthesis of at least two of the three basic flavonoid classes.
Keywords :
Flavonoids , allylation , ring-closing metathesis , Claisen rearrangement , Tebbe methylenation , vinylation , Grubbs’ II catalyst
Journal title :
Tetrahedron Letters
Serial Year :
2012
Journal title :
Tetrahedron Letters
Record number :
1881668
Link To Document :
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