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Enantiomers of an Indole Alkaloid Containing Unusual Dihydrothiopyran and 1,2,4-Thiadiazole Rings from the Root of Isatis indigotica

https://doi.org/10.1021/ol302660t
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.201107204openalex-snapshot
Enantiomeric Natural Products: Occurrence and Biogenesis
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A “Diels‐Alderase” at Last
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Rapid synthesis of 2,5‐disubtituted 1,3,4‐thiadiazoles under microwave irradiation
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Indole alkaloids from the roots of Isatis ingigotica and their antiherpes simplex virus type 2 (HSV-2) activity in vitro
inferredcites →https://doi.org/10.1007/s11426-008-0146-9openalex-snapshot
Isolation, structural determination and cytotoxic activity of two new ceramides from the root of Isatis indigotica
inferredcites →https://doi.org/10.1016/j.cbpa.2011.12.017openalex-snapshot
Current developments and challenges in the search for a naturally selected Diels-Alderase
inferredcites →https://doi.org/10.1016/j.fitote.2010.10.016openalex-snapshot
Novel indole C-glycosides from Isatis indigotica and their potential cytotoxic activity
inferredcites →https://doi.org/10.1016/s0031-9422(00)00316-2openalex-snapshot
The chemical diversity and distribution of glucosinolates and isothiocyanates among plants
inferredcites →https://doi.org/10.1016/s0040-4020(97)00846-6openalex-snapshot
New alkaloids from Isatis indigotica
inferredcites →https://doi.org/10.1016/s0040-4039(00)92744-8openalex-snapshot
Nouveau derive indolique du thiadiazole-1,2,4, isole d'un tunicier (Dendrodoa grossularia).
inferredcites →https://doi.org/10.1016/s0040-4039(01)02015-9openalex-snapshot
Novel indole-type glucosinolates from woad (Isatis tinctoria L.)
inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/jf020468gopenalex-snapshot
Synthesis and Sensorial Properties of Mercaptoaldehydes
inferredcites →https://doi.org/10.1021/jf203321uopenalex-snapshot
Biotransformation of Glucosinolates Epiprogoitrin and Progoitrin to (R)- and (S)-Goitrin in Radix isatidis
inferredcites →https://doi.org/10.1021/jm2016107openalex-snapshot
Discovery of Novel 1,2,4-Thiadiazole Derivatives as Potent, Orally Active Agonists of Sphingosine 1-Phosphate Receptor Subtype 1 (S1P1)
inferredcites →https://doi.org/10.1021/np049662iopenalex-snapshot
Bisindigotin, a TCDD Antagonist from the Chinese Medicinal Herb Isatis indigotica
inferredcites →https://doi.org/10.1021/np3002833openalex-snapshot
Alkaloids from the Root of Isatis indigotica
inferredcites →https://doi.org/10.1021/ol102802uopenalex-snapshot
Spirocurcasone, a Diterpenoid with a Novel Carbon Skeleton from Jatropha curcas
inferredcites →https://doi.org/10.1021/ol701540yopenalex-snapshot
Isatisine A, a Novel Alkaloid with an Unprecedented Skeleton from Leaves of Isatis indigotica
inferredcites →https://doi.org/10.1038/nature09981openalex-snapshot
Enzyme-catalysed [4+2] cycloaddition is a key step in the biosynthesis of spinosyn A
inferredcites →https://doi.org/10.1039/a904107iopenalex-snapshot
Oxidation of methyl groups in the reaction of sulfur homopolyatomic cations with acetonitrile: formation and crystal structure of the novel trithietanylium ring
inferredcites →https://doi.org/10.1039/b515476fopenalex-snapshot
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
inferredcites →https://doi.org/10.1055/s-2006-957604openalex-snapshot
Chemical Constituents ofIsatis indigotica
inferredcites →https://doi.org/10.1055/s-2007-971650openalex-snapshot
Isolation of 2-Hydroxy-3-butenyl Thiocyanate, Epigoitrin, and Adenosine from ‘Banlangen’, Isatis indigotica Root
inferredcites →https://doi.org/10.2174/138527210792927717openalex-snapshot
Determination of Absolute Configuration of Natural Products: Theoretical Calculation of Electronic Circular Dichroism as a Tool

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inferred← citeshttps://doi.org/10.1007/978-3-662-46402-1_4openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules24224033openalex-snapshot
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Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
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