Title of article :
Enantioselective total synthesis of heliespirone B
Author/Authors :
Miyawaki، نويسنده , , Akari and Manabe، نويسنده , , Yuki Shimizu-Yoshida، نويسنده , , Masahiro and Shishido، نويسنده , , Kozo، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2012
Pages :
4
From page :
1236
To page :
1239
Abstract :
The first enantiocontrolled total synthesis of heliespirone B has been accomplished employing a biomimetic intramolecular oxy-Michael reaction followed by the regio- and diastereoselective reduction of the carbonyl function as key steps.
Keywords :
total synthesis , Heliespirone B , Regioselective reduction , diastereoselective reduction , Intramolecular oxy-Michael reaction
Journal title :
Tetrahedron Letters
Serial Year :
2012
Journal title :
Tetrahedron Letters
Record number :
1880232
Link To Document :
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