Title of article :
A highly stereoselective synthesis of the C10–C31 (BCDEF ring) portion of pinnatoxin A
Author/Authors :
Seiichi Nakamura، نويسنده , , Jun Inagaki، نويسنده , , Tomohiro Sugimoto، نويسنده , , Yasuyuki Ura، نويسنده , , Shunichi Hashimoto، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
12
From page :
10375
To page :
10386
Abstract :
An efficient, highly stereoselective synthesis of the C10–C31 (BCDEF ring) portion of pinnatoxin A has been achieved utilizing tandem double hemiketal formation/intramolecular hetero-Michael addition to construct the 6,5,6-dispiroketal (BCD ring) system and subsequent intramolecular ketalization to form the 5,6-bicycloketal (EF ring) system as key steps.
Keywords :
dispiroketal , hemiketal formation , Hetero-Michael addition , internal ketalization
Journal title :
Tetrahedron
Serial Year :
2002
Journal title :
Tetrahedron
Record number :
1083760
Link To Document :
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