N-iodosuccinimide

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

Topic mentions per year

Topic mentions per year

1969-2018
051019692018

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… (More)
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2015
2015
An iron(III)-catalyzed method for the rapid and highly regioselective iodination of arenes has been developed. Use of the… (More)
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2014
2014
Umpolung Amide Synthesis (UmAS) provides direct access to amides from an α-bromo nitroalkane and an amine. Based on its… (More)
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2013
2013
Metal-free cyclization and N-iodosuccinimide-induced electrophilic iodocyclization of readily available 3-aza-1,5-enynes have… (More)
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2010
2010
Cyclodehydration of Bohlmann-Rahtz aminodienone intermediates using N-iodosuccinimide as a Lewis acid proceeds at low temperature… (More)
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2008
2008
Amino acids are very useful as synthetic building blocks for various biologically active compounds. Recently, several… (More)
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2008
2008
The N-iodosuccinimide (NIS) induced nucleosidation of protected natural bases with bicyclo[3.3.0] sugar precursors was… (More)
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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… (More)
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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… (More)
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1996
1996
D-Glucosamine can be readily transformed into 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino+ ++) -D… (More)
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