samarium diiodide

Known as: SmI(2) 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2016
051019962016

Papers overview

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2015
2015
Samarium diiodide mediated cyclizations of N-acylated indole derivatives bearing sulfinyl imine moieties afforded polycyclic… (More)
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2012
2012
Reactions proceeding through open-shell, single-electron pathways offer attractive alternative outcomes to those proceeding… (More)
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Review
2012
Review
2012
Samarium diiodide (SmI(2)) is one of the most important reductive electron transfer reagents available in the laboratory. Key to… (More)
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2011
2011
Samarium diiodide (SmI2) smoothly promotes the cyclizations of suitably substituted carbonyl compounds with styrene subunits… (More)
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2011
2011
The mechanism of samarium diiodide (SmI(2))-induced cyclization of α,β-unsaturated esters and ketones to bicyclic compounds was… (More)
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Review
2009
Review
2009
Introduced by Henri Kagan more than three decades ago, samarium diiodide (SmI(2)) has found increasing application in chemical… (More)
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2009
2009
A flexible diastereoselective approach to trans-(3S)-hydroxyprolinol derivatives is described, which is based on the samarium… (More)
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2007
2007
Experimental and theoretical evidence shows that phthalimides are highly efficient single electron transfer acceptors in… (More)
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2004
2004
[reaction: see text] Samarium diiodide promotes smooth reductive cyclizations of gamma-naphthyl-substituted ketones to afford tri… (More)
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2001
2001
Transformation of acetals into ethers by partial reduction using a samarium diiodide-Lewis acids-acetonitrile system is described… (More)
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