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Amides

Known as: Amides [Chemical/Ingredient], amide 
Organic compounds containing the -CO-NH2 radical. Amides are derived from acids by replacement of -OH by -NH2 or from ammonia by the replacement of H… Expand
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
4.1.2. Intramolecular C-OH Formation 1661 4.1.3. Intermolecular C-OH Formation 1662 4.2. Formation of Ethers 1662 4.2.1. Cyclic… Expand
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Highly Cited
2010
Highly Cited
2010
The selective, direct hydrogenation of amides to the corresponding alcohols and amines with cleavage of the C-N bond was… Expand
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Highly Cited
2010
Highly Cited
2010
The substrate scope, the mechanistic aspects of the gold-catalyzed oxazole synthesis, and substrates with different aliphatic… Expand
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Highly Cited
2009
Highly Cited
2009
The synthesis of secondary amides from primary alcohols and amines has been developed using commercially available [Ru(p-cymene… Expand
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Highly Cited
2007
Highly Cited
2007
Given the widespread importance of amides in biochemical and chemical systems, an efficient synthesis that avoids wasteful use of… Expand
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Highly Cited
2003
Highly Cited
2003
[reaction: see text] A general and efficient copper-catalyzed method for the amidation of vinyl bromides and iodides has been… Expand
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Review
2002
Review
2002
Melatonin was found to be a potent free radical scavenger in 1993. Since then over 800 publications have directly or indirectly… Expand
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Highly Cited
2002
Highly Cited
2002
  • S. Son, B. Lewis
  • Journal of agricultural and food chemistry
  • 2002
  • Corpus ID: 21632693
The structure-activity relationships of synthetic caffeic acid amide and ester analogues as potential antioxidants and free… Expand
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Highly Cited
2000
Highly Cited
2000
[formula: see text] The first general intermolecular C-N bond-forming reactions between aryl halides and amides were realized… Expand
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Highly Cited
1996
Highly Cited
1996
ENDOGENOUS neuromodulatory molecules are commonly coupled to specific metabolic enzymes to ensure rapid signal inactivation. Thus… Expand
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