Title of article :
Synthesis of (−)-neplanocin A with the highest overall yield via an efficient Mitsunobu coupling
Author/Authors :
Benoît Y. Michel، نويسنده , , Peter Strazewski، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Pages :
6
From page :
9836
To page :
9841
Abstract :
Neplanocin A was synthesized in very high isolated yield and purity, in 10 steps from d-ribose via an efficient Mitsunobu coupling using N6-bis-Boc-protected adenine. In fact, this synthesis is a short pathway to enantiopure neplanocin A giving the highest published overall yield.
Keywords :
Antiviral , Antitumor , carbocyclic nucleosides , Mitsunobu coupling , Fürstnerיs catalyst , Metathesis
Journal title :
Tetrahedron
Serial Year :
2007
Journal title :
Tetrahedron
Record number :
1093244
Link To Document :
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