Title of article :
Total synthesis of (–)-diversifolin
Author/Authors :
Nakamura، نويسنده , , Tomoaki and Tsuboi، نويسنده , , Kazuma and Oshida، نويسنده , , Motoko and Nomura، نويسنده , , Tomoko and Nakazaki، نويسنده , , Atsuo and Kobayashi، نويسنده , , Susumu، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Pages :
5
From page :
2835
To page :
2839
Abstract :
First total synthesis of biologically active germacrane-type sesquiterpene (−)-diversifolin has been achieved. The features of the synthesis involve (i) ring-closing metathesis to give a 10-membered carbocycle, (ii) regioselective Mukaiyama aldol reaction of silyl dienol ether with formaldehyde at the α-position, and (iii) lactone transposition of the fully functionalized 11-oxabicyclo[6.2.1]undecane system.
Keywords :
Diversifolin , Lactone transposition , Germacrane-type sesquiterpenes , total synthesis , ring-closing metathesis
Journal title :
Tetrahedron Letters
Serial Year :
2009
Journal title :
Tetrahedron Letters
Record number :
1863993
Link To Document :
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