Title of article :
Synthetic studies of venturicidins: stereoselective synthesis of the C15–C27 segment based on two types of stereospecific epoxide opening reactions
Author/Authors :
Suzuki، نويسنده , , Yuji and Nagumo، نويسنده , , Shinji and Yasui، نويسنده , , Eiko and Mizukami، نويسنده , , Megumi and Miyashita، نويسنده , , Masaaki، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2011
Pages :
4
From page :
6948
To page :
6951
Abstract :
The C15–C27 segment of venturicidins was stereoselectively synthesized by using two types of stereospecific methyl substitution reactions of epoxides and subsequent stereocontrolled methylation reactions of lactone derivatives as the key steps.
Keywords :
Epoxy-unsaturated ester , Venturicidin , Epoxide opening reaction , Epoxy sulfide
Journal title :
Tetrahedron Letters
Serial Year :
2011
Journal title :
Tetrahedron Letters
Record number :
1879750
Link To Document :
https://search.isc.ac/dl/search/defaultta.aspx?DTC=10&DC=1879750
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