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Iodoacetates

Known as: Iodoacetates [Chemical/Ingredient] 
Iodinated derivatives of acetic acid. Iodoacetates are commonly used as alkylating sulfhydryl reagents and enzyme inhibitors in biochemical research.
National Institutes of Health

Papers overview

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2016
2016
The invention discloses aloe-emodin quaternary ammonium salt alkyl iodoacetates with the multiple-related anti-cancer mechanism… Expand
Highly Cited
2008
Highly Cited
2008
The classical Reformatsky reaction, introduced for the first time in 1887, consists of the zinc-induced formation of… Expand
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2004
2004
  • Hui Yu, C. Li
  • The Journal of organic chemistry
  • 2004
  • Corpus ID: 41859708
Atom-transfer radical oligomers of allyl iodoacetates were converted to 4-pentenoic acids upon treatment with zinc. Reactions of… Expand
2004
2004
Triethylborane-initiated atom transfer radical cyclization reactions of various allyl or 3-butenyl iodoacetates could be… Expand
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2004
2004
[reaction: see text] Highly stereodivergent Woodward-Prevost reaction applied to iodoacetates derived from homochiral alpha-amino… Expand
2002
2002
Bis(tributyltin)-initiated atom transfer cyclization reactions of 4-pentenyl iodoacetates (1) at 80 degrees C led to the… Expand
2002
2002
Bis(tributyltin)-initiated atomtransfercyclization reactions of 4-pentenyl iodoacetates(1) at 80℃ led to the formations of 5-(3… Expand
2002
2002
Atom-transfer radical oligomerizations of omega-alkenyl iodoacetates followed by rearrangemental deoligomerization via treatment… Expand
Highly Cited
1985
Highly Cited
1985
Oligonucleotides containing a free sulphydryl group at their 5'-termini have been synthesised and further derivatised with thiol… Expand
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1984
1984
Binding of nucleotides to the high-affinity site of the isolated alpha subunit of normal Escherichia coli F1 adenosine… Expand