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#synthesis — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #synthesis, aggregated by home.social.

  1. I’ve been playing and really enjoying this new release Resilience by Daniel M Karlsson ( @t36s) on @EVEL a lot over the last day or so.

    It's a swooping, swirling, swooning 91 minute continuous piece of utterly sublime computer music, full of sweeping drama and intense emotional resonance. Very highly recommended!

    @ExperimentalMusic

    #ExperimentalMusic #ComputerMusic #Synthesis #DeterministicMusic #DroneMusic #ElectronicMusic social.ordinal.garden/@t36s/11

  2. In the charged dark, endless listening fueled our quiet exchange of truth. By dawn, we had catalyzed into an unbroken whole. 🌌🌅 #Dialogue #Synthesis

  3. 🔴 LIVE NOW ON VORTEX
    📻 Vortex Abyss 🕳️ (Dark ambient, neofolk, shoegaze, immersive)
    ──────────────
    🎵 Angelzoom - Fairyland

    ▶️ Écouter / Listen : VorteX [Radio]
    lesonduvortex.net

    💬 Join us on Discord:
    discord.gg/d82hJZBeDE

    #VortexWave #Angelzoom #Electropop #Synthesis #2000s

  4. Research Unveils Novel Light-Triggered Copper Catalysts for Chemical Reactions

    Scientists made new light-activated copper catalysts for easier chemical reactions. This could change how medicines and materials are made.

    #CopperCatalyst, #ChemicalReactions, #LightActivated, #ChemistryNews, #Synthesis

    newsletter.tf/light-triggered-

  5. Cantai (US) want good choral singers for 2 hr recording session with royalties.
    " singers with a straight-tone technique — minimal-to-no vibrato, clean blending, the kind of voice you'd hear in a chamber choir or an early music ensemble. Not operatic, not pop. All voice parts welcome, soprano through bass.

    If that's you, or someone you know, head to cantai.app and tap the green chat bubble in the bottom-right corner to start a conversation. "
    #AI #choral #synthesis

  6. Cantai (US) want good choral singers for 2 hr recording session with royalties.
    " singers with a straight-tone technique — minimal-to-no vibrato, clean blending, the kind of voice you'd hear in a chamber choir or an early music ensemble. Not operatic, not pop. All voice parts welcome, soprano through bass.

    If that's you, or someone you know, head to cantai.app and tap the green chat bubble in the bottom-right corner to start a conversation. "
    #AI #choral #synthesis

  7. Cantai (US) want good choral singers for 2 hr recording session with royalties.
    " singers with a straight-tone technique — minimal-to-no vibrato, clean blending, the kind of voice you'd hear in a chamber choir or an early music ensemble. Not operatic, not pop. All voice parts welcome, soprano through bass.

    If that's you, or someone you know, head to cantai.app and tap the green chat bubble in the bottom-right corner to start a conversation. "
    #AI #choral #synthesis

  8. Cantai (US) want good choral singers for 2 hr recording session with royalties.
    " singers with a straight-tone technique — minimal-to-no vibrato, clean blending, the kind of voice you'd hear in a chamber choir or an early music ensemble. Not operatic, not pop. All voice parts welcome, soprano through bass.

    If that's you, or someone you know, head to cantai.app and tap the green chat bubble in the bottom-right corner to start a conversation. "
    #AI #choral #synthesis

  9. Cantai (US) want good choral singers for 2 hr recording session with royalties.
    " singers with a straight-tone technique — minimal-to-no vibrato, clean blending, the kind of voice you'd hear in a chamber choir or an early music ensemble. Not operatic, not pop. All voice parts welcome, soprano through bass.

    If that's you, or someone you know, head to cantai.app and tap the green chat bubble in the bottom-right corner to start a conversation. "
    #AI #choral #synthesis

  10. By the way, and for the avoidance of doubt/suspicion: none of the "audio etymology" sequences that I've created and am posting here involve any use of AI, LLM's, neural nets, none of that. All are made from original audio recordings of real people speaking words in their various languages, which are then subjected to good old-fashioned signal processing (speech coding and synthesis). The continua of change are made using straightforward linear interpolation over the space of cepstrograms, which are 2 dimensional matrices encoding the acoustics of the original recordings. Using scripts that I wrote, by hand.

    #acoustics #phonetics #speech #synthesis #audio #maths #linear_algebra

  11. By the way, and for the avoidance of doubt/suspicion: none of the "audio etymology" sequences that I've created and am posting here involve any use of AI, LLM's, neural nets, none of that. All are made from original audio recordings of real people speaking words in their various languages, which are then subjected to good old-fashioned signal processing (speech coding and synthesis). The continua of change are made using straightforward linear interpolation over the space of cepstrograms, which are 2 dimensional matrices encoding the acoustics of the original recordings. Using scripts that I wrote, by hand.

    #acoustics #phonetics #speech #synthesis #audio #maths #linear_algebra

  12. He also hinted at a new class of synthetic antibiotics that is in current development at Roche. Hopefully there are many more new antibiotics in the future. (7/7)

    #Antibiotics #DrugDiscovery #DrugDevelopment #ChemBio #Chemistry #cryoEM #AMR #Resistance #Bacteria #SAR #Synthesis #Zosurabalpin

  13. Excited to share our paper in Journal of Medicinal #Chemistry exploring carbobicyclic nucleoside analogues as potential #antivirals!

    We swapped the ribose oxygen for a carbon in nucleoside analogues and explored this novel scaffold.

    From our library, several compounds showed activity against #HCV, #HSV, #influenza, and #RSV. One uracil-based analogue stood out by inhibiting multiple viruses like #flu and HCV. Modeling suggests it “locks” the viral active site instead of being incorporated into RNA.

    What really surprised us: nucleobases with known antiviral effects (like NHC from molnupiravir) didn’t work in our scaffold—but unmodified uracil did. The scaffold itself changes how these molecules behave.

    Encouragingly, these compounds phosphorylate efficiently in cells without needing prodrugs, don't inhibit human polymerases, and our #synthesis is efficient: 28 pyrimidine and 35 purine analogues from just two intermediates in under 10 steps.

    Huge thanks to all collaborators and colleagues who made this work possible!

    pubs.acs.org/doi/10.1021/acs.j

    J. Med. Chem. 2026, 69, 5, 5501–5539.

    #research #science #drug

  14. Excited to share our paper in Journal of Medicinal #Chemistry exploring carbobicyclic nucleoside analogues as potential #antivirals!

    We swapped the ribose oxygen for a carbon in nucleoside analogues and explored this novel scaffold.

    From our library, several compounds showed activity against #HCV, #HSV, #influenza, and #RSV. One uracil-based analogue stood out by inhibiting multiple viruses like #flu and HCV. Modeling suggests it “locks” the viral active site instead of being incorporated into RNA.

    What really surprised us: nucleobases with known antiviral effects (like NHC from molnupiravir) didn’t work in our scaffold—but unmodified uracil did. The scaffold itself changes how these molecules behave.

    Encouragingly, these compounds phosphorylate efficiently in cells without needing prodrugs, don't inhibit human polymerases, and our #synthesis is efficient: 28 pyrimidine and 35 purine analogues from just two intermediates in under 10 steps.

    Huge thanks to all collaborators and colleagues who made this work possible!

    pubs.acs.org/doi/10.1021/acs.j

    J. Med. Chem. 2026, 69, 5, 5501–5539.

    #research #science #drug

  15. Excited to share our paper in Journal of Medicinal #Chemistry exploring carbobicyclic nucleoside analogues as potential #antivirals!

    We swapped the ribose oxygen for a carbon in nucleoside analogues and explored this novel scaffold.

    From our library, several compounds showed activity against #HCV, #HSV, #influenza, and #RSV. One uracil-based analogue stood out by inhibiting multiple viruses like #flu and HCV. Modeling suggests it “locks” the viral active site instead of being incorporated into RNA.

    What really surprised us: nucleobases with known antiviral effects (like NHC from molnupiravir) didn’t work in our scaffold—but unmodified uracil did. The scaffold itself changes how these molecules behave.

    Encouragingly, these compounds phosphorylate efficiently in cells without needing prodrugs, don't inhibit human polymerases, and our #synthesis is efficient: 28 pyrimidine and 35 purine analogues from just two intermediates in under 10 steps.

    Huge thanks to all collaborators and colleagues who made this work possible!

    pubs.acs.org/doi/10.1021/acs.j

    J. Med. Chem. 2026, 69, 5, 5501–5539.

    #research #science #drug

  16. Excited to share our paper in Journal of Medicinal #Chemistry exploring carbobicyclic nucleoside analogues as potential #antivirals!

    We swapped the ribose oxygen for a carbon in nucleoside analogues and explored this novel scaffold.

    From our library, several compounds showed activity against #HCV, #HSV, #influenza, and #RSV. One uracil-based analogue stood out by inhibiting multiple viruses like #flu and HCV. Modeling suggests it “locks” the viral active site instead of being incorporated into RNA.

    What really surprised us: nucleobases with known antiviral effects (like NHC from molnupiravir) didn’t work in our scaffold—but unmodified uracil did. The scaffold itself changes how these molecules behave.

    Encouragingly, these compounds phosphorylate efficiently in cells without needing prodrugs, don't inhibit human polymerases, and our #synthesis is efficient: 28 pyrimidine and 35 purine analogues from just two intermediates in under 10 steps.

    Huge thanks to all collaborators and colleagues who made this work possible!

    pubs.acs.org/doi/10.1021/acs.j

    J. Med. Chem. 2026, 69, 5, 5501–5539.

    #research #science #drug

  17. Excited to share our paper in Journal of Medicinal #Chemistry exploring carbobicyclic nucleoside analogues as potential #antivirals!

    We swapped the ribose oxygen for a carbon in nucleoside analogues and explored this novel scaffold.

    From our library, several compounds showed activity against #HCV, #HSV, #influenza, and #RSV. One uracil-based analogue stood out by inhibiting multiple viruses like #flu and HCV. Modeling suggests it “locks” the viral active site instead of being incorporated into RNA.

    What really surprised us: nucleobases with known antiviral effects (like NHC from molnupiravir) didn’t work in our scaffold—but unmodified uracil did. The scaffold itself changes how these molecules behave.

    Encouragingly, these compounds phosphorylate efficiently in cells without needing prodrugs, don't inhibit human polymerases, and our #synthesis is efficient: 28 pyrimidine and 35 purine analogues from just two intermediates in under 10 steps.

    Huge thanks to all collaborators and colleagues who made this work possible!

    pubs.acs.org/doi/10.1021/acs.j

    J. Med. Chem. 2026, 69, 5, 5501–5539.

    #research #science #drug

  18. How do you pick the right target molecule for a total synthesis program?

    At #Lunteren2026, Dirk Trauner gave an inspiring lecture with a lot of thought-provoking potential reasons to select a target molecule in combination with many insights into fascinating completed total syntheses.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Synthesis

  19. How do you pick the right target molecule for a total synthesis program?

    At #Lunteren2026, Dirk Trauner gave an inspiring lecture with a lot of thought-provoking potential reasons to select a target molecule in combination with many insights into fascinating completed total syntheses.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Synthesis

  20. How do you pick the right target molecule for a total synthesis program?

    At #Lunteren2026, Dirk Trauner gave an inspiring lecture with a lot of thought-provoking potential reasons to select a target molecule in combination with many insights into fascinating completed total syntheses.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Synthesis

  21. How do you pick the right target molecule for a total synthesis program?

    At #Lunteren2026, Dirk Trauner gave an inspiring lecture with a lot of thought-provoking potential reasons to select a target molecule in combination with many insights into fascinating completed total syntheses.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Synthesis

  22. How do you pick the right target molecule for a total synthesis program?

    At #Lunteren2026, Dirk Trauner gave an inspiring lecture with a lot of thought-provoking potential reasons to select a target molecule in combination with many insights into fascinating completed total syntheses.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Synthesis

  23. Interesting talk by Peter Fodran from the University of Groningen at #Lunteren2026. He talked about his group's work on the efficient and #MedChem friendly synthesis of privileged scaffolds for drug discovery.

    fodranlab.com/
    #Chemistry #ChemBio #DrugDiscovery #Synthesis

  24. Interesting talk by Peter Fodran from the University of Groningen at #Lunteren2026. He talked about his group's work on the efficient and #MedChem friendly synthesis of privileged scaffolds for drug discovery.

    fodranlab.com/
    #Chemistry #ChemBio #DrugDiscovery #Synthesis

  25. Interesting talk by Peter Fodran from the University of Groningen at #Lunteren2026. He talked about his group's work on the efficient and #MedChem friendly synthesis of privileged scaffolds for drug discovery.

    fodranlab.com/
    #Chemistry #ChemBio #DrugDiscovery #Synthesis

  26. Interesting talk by Peter Fodran from the University of Groningen at #Lunteren2026. He talked about his group's work on the efficient and #MedChem friendly synthesis of privileged scaffolds for drug discovery.

    fodranlab.com/
    #Chemistry #ChemBio #DrugDiscovery #Synthesis

  27. Interesting talk by Peter Fodran from the University of Groningen at #Lunteren2026. He talked about his group's work on the efficient and #MedChem friendly synthesis of privileged scaffolds for drug discovery.

    fodranlab.com/
    #Chemistry #ChemBio #DrugDiscovery #Synthesis

  28. As an organic chemist, should you specialize in synthesis method development or total synthesis?

    In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.

    #Chemistry #Synthesis #Catalysis

  29. As an organic chemist, should you specialize in synthesis method development or total synthesis?

    In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.

    #Chemistry #Synthesis #Catalysis

  30. As an organic chemist, should you specialize in synthesis method development or total synthesis?

    In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.

    #Chemistry #Synthesis #Catalysis

  31. As an organic chemist, should you specialize in synthesis method development or total synthesis?

    In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.

    #Chemistry #Synthesis #Catalysis

  32. As an organic chemist, should you specialize in synthesis method development or total synthesis?

    In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.

    #Chemistry #Synthesis #Catalysis

  33. Interesting talk by Géraldine Masson at #Lunteren2026. She gave a presentation with the title "Chiral Brønsted Acid–Driven Enantio- and Regioselective Transformations of Polyunsaturated Systems toward Complex Molecular Architectures".

    #Chemistry #Synthesis #Catalysis

  34. Interesting talk by Géraldine Masson at #Lunteren2026. She gave a presentation with the title "Chiral Brønsted Acid–Driven Enantio- and Regioselective Transformations of Polyunsaturated Systems toward Complex Molecular Architectures".

    #Chemistry #Synthesis #Catalysis

  35. Interesting talk by Géraldine Masson at #Lunteren2026. She gave a presentation with the title "Chiral Brønsted Acid–Driven Enantio- and Regioselective Transformations of Polyunsaturated Systems toward Complex Molecular Architectures".

    #Chemistry #Synthesis #Catalysis

  36. Interesting talk by Géraldine Masson at #Lunteren2026. She gave a presentation with the title "Chiral Brønsted Acid–Driven Enantio- and Regioselective Transformations of Polyunsaturated Systems toward Complex Molecular Architectures".

    #Chemistry #Synthesis #Catalysis

  37. Interesting talk by Géraldine Masson at #Lunteren2026. She gave a presentation with the title "Chiral Brønsted Acid–Driven Enantio- and Regioselective Transformations of Polyunsaturated Systems toward Complex Molecular Architectures".

    #Chemistry #Synthesis #Catalysis

  38. Interesting talk by Antonio Echavarren at #Lunteren2026. He talked about the use of gold-carbene catalysis to perform complex and enantioselective transformations in organic synthesis.

    pubs.acs.org/doi/10.1021/jacsa
    #Synthesis #OrganicChemistry #Chemistry #Catalysis