Title of article :
Total synthesis and absolute stereochemistry of plakortone E
Author/Authors :
Akiyama، نويسنده , , Megumi and Isoda، نويسنده , , Yuichi and Nishimoto، نويسنده , , Masato and Narazaki، نويسنده , , Maiko and Oka، نويسنده , , Hiroaki and Kuboki، نويسنده , , Atsuhito and Ohira، نويسنده , , Susumu، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2006
Pages :
4
From page :
2287
To page :
2290
Abstract :
The absolute stereochemistry of plakortone E, a cytotoxic metabolite of the Caribbean sponge, was established to be 1, by the synthesis of the racemic C-8 epimer (±)-2 and then of (−)-1 itself, which was identical with the natural compound.
Keywords :
Plakortone E , alkylidenecarbene , Absolute stereochemistry , C–H insertion
Journal title :
Tetrahedron Letters
Serial Year :
2006
Journal title :
Tetrahedron Letters
Record number :
1849395
Link To Document :
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