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lentiginosine

Known as: 1,2-Indolizinediol, octahydro-, (1S-(1alpha,2beta,8aalpha))-, 1,2-dihydroxyindolizidine 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Alkaloids

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Hsp 90 Activity Modulation by Plant Secondary Metabolites
Hsp90 is an evolutionarily conserved adenosine triphosphate-dependent molecular chaperone and is one of the most abundant… 
2012
2012
Total Synthesis Of Palmerolide A, Dihydroconduritols And Lentiginosine
2010
2010
A Facile Synthesis of Lentiginosine Analogues Based on a Highly Regio‐ and Diastereoselective Allylic Amination Using Chlorosulfonyl Isocyanate
The concise synthesis of the lentiginosine analogues pyrrolizidine alkaloid 2 and pyrroloazepine alkaloid 3 has been achieved… 
2007
2007
A novel class of glycosidase inhibitors: structures related to australine, lentiginosine, salacinol and swainsonine
This thesis focuses on the design and syntheses of the sulfonium-ion analogues of australine, lentiginosine, swainsonine, and… 
2005
2005
Stereoselective allyl amine synthesis through enantioselective addition of diethylzinc and [1,3]-chirality transfer: synthesis of lentiginosine and polyoxamic acid derivative.
A new synthetic method for the preparation of allyl amines has been developed. The key steps of this method are enantioselective… 
2005
2005
Free energy perturbation calculations on glucosidase-inhibitor complexes.
Free energy perturbation studies have been performed on Glucoamylase II (471) from Aspergillus awamori var. X100 complexed with… 
Review
2004
Review
2004
Indolizidine and quinolizidine alkaloids.
  • J. Michael
  • Natural product reports (Print)
  • 2004
  • Corpus ID: 33623253
This review covers the isolation, structure determination, synthesis, chemical transformations and biological activity of… 
Review
2001
Review
2001
Indolizidine and quinolizidine alkaloids.
  • J. Michael
  • Natural product reports (Print)
  • 2001
  • Corpus ID: 27406961
This review covers the isolation, structure determination, synthesis, chemical transformations and biological activity of… 
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