Title of article :
Ring closing metathesis for the formation of medium ring ethers: the total synthesis of (−)-isolaurallene
Author/Authors :
Michael A. Crimmins، نويسنده , , Kyle A Emmitte، نويسنده , , Allison L. Choy، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
18
From page :
1817
To page :
1834
Abstract :
The total synthesis of the marine metabolite (−)-isolaurallene is described. Two approaches to the core nine-membered ether are presented both of which are based on a ring closing metathesis to close the cyclic ether.
Keywords :
asymmetric aldol , asymmetric alkylation , oxonene , Metathesis , marine natural products , isolaurallene
Journal title :
Tetrahedron
Serial Year :
2002
Journal title :
Tetrahedron
Record number :
1082863
Link To Document :
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