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allysine aldol

Known as: Undecanedioic acid, 2,10-diamino-5-formyl-6-hydroxy- 
National Institutes of Health

Papers overview

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2015
2015
An eleven-step synthesis of (±)-spongiolactone from 1,3-cyclohexanedione is reported that relies on a diastereoselective… Expand
Highly Cited
2012
Highly Cited
2012
Dyotropic rearrangements of fused, tricyclic β-lactones are described that proceed via unprecedented stereospecific, 1,2-acyl… Expand
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2012
2012
A formal synthesis of merrilactone A has been completed using a domino 1,4-addition-aldol process as the key step. Both iodo- and… Expand
Highly Cited
2010
Highly Cited
2010
The aldol reaction is one of the most ubiquitous in synthetic organic chemistry. The vinylogous extension of this fundamental C C… Expand
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Highly Cited
2010
Highly Cited
2010
An advance in the asymmetric, nucleophile-catalyzed aldol lactonization process with keto acid substrates is described. 
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Highly Cited
2010
Highly Cited
2010
Two novel domino NHC-catalyzed spirocyclizations are described herein, enabling the rapid construction of three new carbon-carbon… Expand
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Highly Cited
2010
Highly Cited
2010
A double diastereoselective variant of the nucleophile-catalyzed aldol lactonization (NCAL) process is described. This strategy… Expand
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2008
2008
  • H. Li, T. Loh
  • Journal of the American Chemical Society
  • 2008
  • Corpus ID: 29487365
Mukaiyama-Aldol and Prins reactions have been identified as highly efficient methods in C-C bond formation since they were… Expand
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2005
2005
A new tandem aldol-allylation reaction employing ketone-derived enolates has been developed that leads to the rapid… Expand
Highly Cited
1973
Highly Cited
1973
Abstract Reduction of insoluble collagens from bone, skin, and tendon with NaB3H4 produced several radioactive substances which… Expand
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