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N-iodosuccinimide

Known as: 1-iodo-2,5-pyrrolidinedione 
 
National Institutes of Health

Papers overview

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2017
2017
4-Aryl and 4-alkyl substituted 3-iodoquinolines could be smoothly obtained in one pot by treating N-tosyl-2-propynylamines with… Expand
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2016
2016
Polysubstituted pyrrolin-4-ones have been efficiently synthesized from readily available 1-(N-sulfonylazetidin-2-yl) ynones via… Expand
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2013
2013
Novel thiophene-fused 1,1’-biazulene derivative was prepared by the reaction of azuleno[1,2-b]thiophene with N-iodosuccinimide… Expand
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2010
2010
Cyclodehydration of Bohlmann-Rahtz aminodienone intermediates using N‑iodosuccinimide as a Lewis acid proceeds at low temperature… Expand
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2008
2008
Amino acids are very useful as synthetic building blocks for various biologically active compounds. Recently, several… Expand
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2007
2007
Imines react with N-iodosuccinimide (NIS) to afford unexpected 1 : 1 complexes and the structure of one of these was determined… Expand
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2007
2007
Dissolution of N-iodosuccinimide in sulfuric acid gives rise to electrophilic iodine-containing species which are capable of… Expand
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2003
2003
The effect of 4,6-O-benzylidene acetals, 4,6-O-phenylboronate esters, and 4,6-O-polystyrylboronate esters on the… Expand
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Highly Cited
2002
Highly Cited
2002
Abstract A variety of aromatics compounds substituted with methoxy or methyl groups were regioselectively iodinated with N… Expand
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1969
1969
N-Iodosuccinimide in sulphuric acid and a mixture of silver sulphate and iodine in sulphuric acid both convert fluorenone into 2… Expand
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