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SCH 351448

Known as: SCH-351448, SCH351448 
 
National Institutes of Health

Papers overview

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2011
2011
An efficient formal synthesis of SCH 351448 was accomplished through the tandem cross-metathesis (CM)/oxa-Michael, the 1,4-syn… Expand
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2008
2008
The synthesis and absolute configuration of SCH 351448, an interesting ionophoric natural product, are reported herein. Mukaiyama… Expand
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2006
2006
[structure: see text] A stereoselective synthesis of SCH 351448 has been completed. Twelve of the fourteen stereogenic centers… Expand
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2005
2005
(+)-SCH 351448 (Na+ salt A) was synthesized employing ring-closing olefin metathesis reaction of an open diene diester… Expand
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2005
2005
 
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2004
2004
Total synthesis of SCH 351448 was accomplished employing the ring-closing olefin metathesis reaction for the preparation of the… Expand
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2004
2004
 
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2002
2002
[structure: see text] A convergent, stereoselective assembly of the C1-C21 (C1'-C21') fragment of SCH 351448, a 28-membered bis… Expand
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