Results 11 to 20 of about 18,265 (273)

Caylobolide B: Structure Revision, Total Synthesis, Biological Characterization, and Discovery of New Analogues. [PDF]

open access: yesAngew Chem Int Ed Engl
Marine polyhydroxylated macrolides’ drug discovery potential is limited by structural complexity and scarce material supply, hindering structure assignment, synthesis, and biological studies. Here, we present an integrated workflow that combines chemogenomic profiling, ultra‐high‐resolution NMR‐guided structural revision and stereochemical assignment ...
George MRP   +9 more
europepmc   +3 more sources

Stereoselective Total Synthesis of (+)-Giganin and Its C10 Epimer by Using Late-Stage LithiationBorylation Methodology [PDF]

open access: green, 2013
Alali   +55 more
core   +4 more sources

Distinguishing Epimers Through Raman Optical Activity [PDF]

open access: yesThe Journal of Physical Chemistry A, 2016
The Raman optical activity spectra of the epimers β-D-glucose and β-D-galactose, two monosaccharides of biological importance, have been calculated using molecular dynamics combined with a quantum mechanics/molecular mechanics approach. Good agreement between theoretical and experimental spectra is observed for both monosaccharides.
Mutter, Shaun   +4 more
openaire   +5 more sources

Anti-Angiogenic Properties of Ginsenoside Rg3

open access: yesMolecules, 2020
Ginsenoside Rg3 (Rg3) is a member of the ginsenoside family of chemicals extracted from Panax ginseng. Like other ginsenosides, Rg3 has two epimers: 20(S)-ginsenoside Rg3 (SRg3) and 20(R)-ginsenoside Rg3 (RRg3).
Maryam Nakhjavani   +4 more
doaj   +1 more source

Chiral Separation, Configuration Confirmation and Bioactivity Determination of the Stereoisomers of Hesperidin and Narirutin in Citrus reticulata Blanco

open access: yesMolecules, 2023
Hesperidin and narirutin are a class of flavanone glycosides, which are the main active constituents in Citrus reticulata Blanco. In the present study, a chiral HPLC-UV method with amylose tris(3,5-dimethylphenylcarbamate) as a stationary phase under a ...
Bingtong Jiang   +3 more
doaj   +1 more source

Epimerisation in Peptide Synthesis

open access: yesMolecules, 2023
Epimerisation is basically a chemical conversion that includes the transformation of an epimer into another epimer or its chiral partner. Epimerisation of amino acid is a side reaction that sometimes happens during peptide synthesis.
Suleman Duengo   +4 more
doaj   +1 more source

Total Synthesis of 6-Deoxydihydrokalafungin, a Key Biosynthetic Precursor of Actinorhodin, and Its Epimer

open access: yesMolecules, 2021
In this article, we report the total synthesis of 6-deoxydihydrokalafungin (DDHK), a key biosynthetic intermediate of a dimeric benzoisochromanequinone antibiotic, actinorhodin (ACT), and its epimer, epi-DDHK.
Takuya Kumamoto   +6 more
doaj   +1 more source

Epimers with distinct mechanical behaviours

open access: yesCrystEngComm, 2021
Two epimeric series of esters exhibit distinct mechanical behaviour: brittle crystals for one series and ductile crystals for the other series.
Udaya B. Rao Khandavilli   +5 more
openaire   +2 more sources

Bioinspired Synthesis of Twin abeo-Steroids Bufogargarizins A and B via a Divergent Intramolecular Aldol Addition Reaction. [PDF]

open access: yesAngew Chem Int Ed Engl
Twin natural products. This manuscript describes a concise biomimetic synthesis of twin abeo‐steroids bufogargarizins A and B with an unusual [7.5.6.5] and [5.7.6.5] skeletons in 19 steps (LLS). The described synthetic approach features the application of a bioinspired regiodivergent intramolecular aldol addition reaction and a selective singlet oxygen‐
Surma ZJ   +7 more
europepmc   +3 more sources

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