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#organicsynthesis

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Hacker News<p>Artificial photosynthesis directed toward organic synthesis</p><p><a href="https://www.nature.com/articles/s41467-025-56374-z" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">nature.com/articles/s41467-025</span><span class="invisible">-56374-z</span></a></p><p><a href="https://mastodon.social/tags/HackerNews" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>HackerNews</span></a> <a href="https://mastodon.social/tags/ArtificialPhotosynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>ArtificialPhotosynthesis</span></a> <a href="https://mastodon.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a> <a href="https://mastodon.social/tags/RenewableEnergy" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>RenewableEnergy</span></a> <a href="https://mastodon.social/tags/GreenChemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>GreenChemistry</span></a> <a href="https://mastodon.social/tags/Innovation" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Innovation</span></a></p>
UnivGroJobs (By: Jako Jellema)<p><a href="https://mastodon.education/tags/Postdoc" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Postdoc</span></a> in <a href="https://mastodon.education/tags/MachineLearning" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>MachineLearning</span></a> for Oligopeptide Design (1.0 FTE)</p><p><a href="https://www.rug.nl/about-ug/work-with-us/job-opportunities/?details=00347-02S000B23P" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">rug.nl/about-ug/work-with-us/j</span><span class="invisible">ob-opportunities/?details=00347-02S000B23P</span></a></p><p>Department: Faculty of <a href="https://mastodon.education/tags/Science" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Science</span></a> and <a href="https://mastodon.education/tags/Engineering" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Engineering</span></a> <br><a href="https://mastodon.education/tags/UniversityOfGroningen" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>UniversityOfGroningen</span></a> <a href="https://mastodon.education/tags/Groningen" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Groningen</span></a> <a href="https://mastodon.education/tags/FediHire" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>FediHire</span></a> </p><p>For more info you can contact: <br>R. (Robert) Pollice, Dr</p><p>Assistant Professor for Computer-Aided <a href="https://mastodon.education/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a><br><a href="https://www.rug.nl/staff/r.pollice/?lang=en" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">rug.nl/staff/r.pollice/?lang=e</span><span class="invisible">n</span></a></p><p>Apply before: February 28, 2025</p>
Beilstein-Institut<p>Submission deadline extended to 📅 Jan 15, 2025 </p><p>Invitation to submit to the thematic issue “<a href="https://hessen.social/tags/Photocatalysis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Photocatalysis</span></a> and <a href="https://hessen.social/tags/photochemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>photochemistry</span></a> in <a href="https://hessen.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a>” edited by Timothy Noël, University of Amsterdam and Bartholomäus (Bart) Pieber, Institute of Science and Technology Austria in the Beilstein Journal of Organic Chemistry. </p><p>🔗 <a href="https://www.beilstein-journals.org/bjoc/series/139?M=y" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">beilstein-journals.org/bjoc/se</span><span class="invisible">ries/139?M=y</span></a><br><a href="https://hessen.social/tags/BJOC" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>BJOC</span></a> 💎🔓</p>
Beilstein-Institut<p>There’s still time to submit your latest research to the thematic issue “<a href="https://hessen.social/tags/Photocatalysis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Photocatalysis</span></a> and <a href="https://hessen.social/tags/photochemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>photochemistry</span></a> in <a href="https://hessen.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a>” edited by Timothy Noël, University of Amsterdam and Bartholomäus (Bart) Pieber, Institute of Science and Technology Austria in the Beilstein Journal of Organic Chemistry. <br>Submission deadline: 📅 Oct 15, 2024</p><p>🔗 <a href="https://www.beilstein-journals.org/bjoc/series/139?M=y" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">beilstein-journals.org/bjoc/se</span><span class="invisible">ries/139?M=y</span></a></p><p><a href="https://hessen.social/tags/BJOC" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>BJOC</span></a> 💎🔓</p>
Beilstein-Institut<p>You are cordially invited to submit your latest research to the new thematic issue “<a href="https://hessen.social/tags/Photocatalysis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Photocatalysis</span></a> and <a href="https://hessen.social/tags/photochemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>photochemistry</span></a> in <a href="https://hessen.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a>” edited by Timothy Noël, University of Amsterdam and Bartholomäus (Bart) Pieber, Institute of Science and Technology Austria in the Beilstein Journal of Organic Chemistry. </p><p>Submission deadline: 📅 Oct 15, 2024<br><a href="https://hessen.social/tags/BJOC" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>BJOC</span></a> 💎🔓</p><p>🔗 <a href="https://www.beilstein-journals.org/bjoc/series/139?M=y" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">beilstein-journals.org/bjoc/se</span><span class="invisible">ries/139?M=y</span></a></p>
ChemistryViews<p>Straightforward Path to Cyanoformamides</p><p>Dimethylphenylsilylcyanide used as a cyanide source for addition to widely available isocyanates</p><p><a href="https://www.chemistryviews.org/straightforward-path-to-cyanoformamides/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/straightfor</span><span class="invisible">ward-path-to-cyanoformamides/</span></a></p><p><a href="https://mstdn.social/tags/cyanidechemistry" class="mention hashtag" rel="tag">#<span>cyanidechemistry</span></a> <a href="https://mstdn.social/tags/orgchem" class="mention hashtag" rel="tag">#<span>orgchem</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a></p>
ChemistryViews<p>Electrophilic Cyclopropenyl-Gold(III) Species</p><p>Synthetic equivalents of σ-type cyclopropenium cations accessed using gold catalysis</p><p><a href="https://www.chemistryviews.org/electrophilic-cyclopropenyl-goldiii-species/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/electrophil</span><span class="invisible">ic-cyclopropenyl-goldiii-species/</span></a></p><p><a href="https://mstdn.social/tags/cyclopropenes" class="mention hashtag" rel="tag">#<span>cyclopropenes</span></a> <a href="https://mstdn.social/tags/goldcatalysis" class="mention hashtag" rel="tag">#<span>goldcatalysis</span></a> <a href="https://mstdn.social/tags/orgchem" class="mention hashtag" rel="tag">#<span>orgchem</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/science" class="mention hashtag" rel="tag">#<span>science</span></a> <a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a></p>
ChemistryViews<p>Using Light to Edit the Molecular Skeleton of Pyridines</p><p>🌟 One-pot photochemical method transforms pyridines into bicyclic pyrazolines, pyrazoles, or 1,2-diazepines</p><p><a href="https://www.chemistryviews.org/using-light-to-edit-the-molecular-skeleton-of-pyridines/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/using-light</span><span class="invisible">-to-edit-the-molecular-skeleton-of-pyridines/</span></a></p><p>#<a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/organicchem" class="mention hashtag" rel="tag">#<span>organicchem</span></a></p>
Beilstein-Institut<p>You are cordially invited to submit your latest research to the new thematic issue “<a href="https://hessen.social/tags/Photocatalysis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Photocatalysis</span></a> and <a href="https://hessen.social/tags/photochemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>photochemistry</span></a> in <a href="https://hessen.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a>” edited by Timothy Noël, University of Amsterdam and Bartholomäus (Bart) Pieber, Institute of Science and Technology Austria in the Beilstein Journal of Organic Chemistry.<br> <br>Submission deadline: 📅 Oct 15, 2024<br>👉 <a href="https://www.beilstein-journals.org/bjoc/series/139?M=y" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">beilstein-journals.org/bjoc/se</span><span class="invisible">ries/139?M=y</span></a></p><p><a href="https://hessen.social/tags/BJOC" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>BJOC</span></a> 💎🔓</p>
katch wreck<p>"...Mg(OAc)2 outcompetes the interaction between Ag and the <a href="https://mastodon.social/tags/aldehyde" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>aldehyde</span></a>, thereby tuning the Ag surface for selective product formation. Data are consistent with an increased population of Mg-bound aldehyde facilitating the addition of a carbon-centred radical (product of Ag-electrocatalysed organic halide reduction) to the <a href="https://mastodon.social/tags/carbonyl" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>carbonyl</span></a>. <a href="https://mastodon.social/tags/Electron" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Electron</span></a> transfer from Ag to the resultant alkoxy radical yields the desired alcohol."</p><p><a href="https://mastodon.social/tags/electroChemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>electroChemistry</span></a> <a href="https://mastodon.social/tags/organicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>organicSynthesis</span></a> <a href="https://mastodon.social/tags/catalysis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>catalysis</span></a></p><p><a href="https://www.nature.com/articles/s41929-023-01073-5" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">nature.com/articles/s41929-023</span><span class="invisible">-01073-5</span></a></p>
Lives in Chemistry<p><a href="https://mastodon.social/tags/LiC_Previews" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>LiC_Previews</span></a>:<br>We are working on the LARRY&nbsp;E. OVERMAN <a href="https://mastodon.social/tags/autobiography" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>autobiography</span></a> about “Designing Synthetic Methods and <a href="https://mastodon.social/tags/NaturalProducts" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>NaturalProducts</span></a> <a href="https://mastodon.social/tags/Synthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Synthesis</span></a>” that will be released in Spring 2024. Born in 1943 in Chicago, he had joined the newly founded Faculty of Chemistry @UCIrvine in 1971. It became his homebase for more than 50&nbsp;years until his retirement as Distinguished Professor of Chemistry, Emeritus. Larry is most known for the Overman <a href="https://mastodon.social/tags/rearrangement" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>rearrangement</span></a>.</p><p><a href="https://mastodon.social/tags/LiC_advent2023" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>LiC_advent2023</span></a> <a href="https://mastodon.social/tags/SyntheticMethods" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>SyntheticMethods</span></a> <a href="https://mastodon.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a></p>
Beilstein-Institut<p>Meet our Managing Editor Dr. Marc Kielmann <span class="h-card" translate="no"><a href="https://mstdn.science/@mkielmann" class="u-url mention" rel="nofollow noopener" target="_blank">@<span>mkielmann</span></a></span> at the 15th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-15) in Kyoto, Japan 🇯🇵, next week.</p><p><a href="https://hessen.social/tags/IKCOC15" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>IKCOC15</span></a> <a href="https://hessen.social/tags/ikcoc" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>ikcoc</span></a> <a href="https://hessen.social/tags/kyoto" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>kyoto</span></a> <a href="https://hessen.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a> <a href="https://hessen.social/tags/OrganicChemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicChemistry</span></a> <a href="https://hessen.social/tags/synthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>synthesis</span></a> </p><p>➡️ <a href="https://www.beilstein-journals.org/bjoc/news/6YJWZFECZRHMKSWLGGXW2BTPUE/?M=y" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">beilstein-journals.org/bjoc/ne</span><span class="invisible">ws/6YJWZFECZRHMKSWLGGXW2BTPUE/?M=y</span></a></p><p><a href="https://hessen.social/tags/BJOC" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>BJOC</span></a> <a href="https://hessen.social/tags/DiamondOpenAccess" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>DiamondOpenAccess</span></a> <a href="https://hessen.social/tags/DOA" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>DOA</span></a> 💎 🔓</p>
Beilstein-Institut<p>Meet our Managing Editor Dr. Marc Kielmann <span class="h-card" translate="no"><a href="https://mstdn.science/@mkielmann" class="u-url mention" rel="nofollow noopener" target="_blank">@<span>mkielmann</span></a></span> at the 15th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-15) in Kyoto, Japan 🇯🇵.</p><p>➡️ <a href="https://www.beilstein-journals.org/bjoc/news/6YJWZFECZRHMKSWLGGXW2BTPUE/?M=y" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">beilstein-journals.org/bjoc/ne</span><span class="invisible">ws/6YJWZFECZRHMKSWLGGXW2BTPUE/?M=y</span></a></p><p><a href="https://hessen.social/tags/IKCOC15" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>IKCOC15</span></a> <a href="https://hessen.social/tags/ikcoc" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>ikcoc</span></a> <a href="https://hessen.social/tags/kyoto" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>kyoto</span></a> <a href="https://hessen.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a> <a href="https://hessen.social/tags/OrganicChemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicChemistry</span></a> <a href="https://hessen.social/tags/synthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>synthesis</span></a> </p><p><a href="https://hessen.social/tags/BJOC" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>BJOC</span></a> <a href="https://hessen.social/tags/DiamondOpenAccess" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>DiamondOpenAccess</span></a> <a href="https://hessen.social/tags/DOA" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>DOA</span></a> 💎 🔓</p>
ChemistryViews<p>Mechanochemical Synthesis of Corannulene: Curved polycyclic aromatic hydrocarbon synthesized via ball milling </p><p><a href="https://bit.ly/45xCKPE" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">bit.ly/45xCKPE</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/organicchemistry" class="mention hashtag" rel="tag">#<span>organicchemistry</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/ballmill" class="mention hashtag" rel="tag">#<span>ballmill</span></a></p>
ChemistryViews<p>α-Alkylation of Saturated Cyclic Ketones: Amine-free, directing-group-free transformation using quantum dots as a photocatalyst </p><p><a href="https://bit.ly/45x5N64" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">bit.ly/45x5N64</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/reserch" class="mention hashtag" rel="tag">#<span>reserch</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/cyclic" class="mention hashtag" rel="tag">#<span>cyclic</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/scicon" class="mention hashtag" rel="tag">#<span>scicon</span></a></p>
Beilstein-Institut<p>📌 Check out this Editorial by our Guest Editor Philipp Heretsch as well as the other contributions to his and Andreas Kirschning’s Thematic Issue “Platform and enabling technologies in <a href="https://home.social/tags/OrganicSynthesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>OrganicSynthesis</span></a>”</p><p>Download the complete issue with just one click: 👉<a href="https://www.beilstein-journals.org/bjoc/series/114/?M=y" rel="nofollow noopener" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">beilstein-journals.org/bjoc/se</span><span class="invisible">ries/114/?M=y</span></a></p><p><a href="https://home.social/tags/FlowChemistry" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>FlowChemistry</span></a> <a href="https://home.social/tags/MethodsDevelopment" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>MethodsDevelopment</span></a> <a href="https://home.social/tags/ReactorDesign" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>ReactorDesign</span></a></p><p><a href="https://home.social/tags/DiamondOpenAccess" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>DiamondOpenAccess</span></a> 💎🔓 <a href="https://home.social/tags/BJOC" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>BJOC</span></a></p>
ChemistryViews<p>Total Synthesis of Chaetoglobin A: Dimeric alkaloid from a fungus has a chiral axis connecting two azaphilone systems </p><p><a href="https://bit.ly/45sts7F" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">bit.ly/45sts7F</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/scicon" class="mention hashtag" rel="tag">#<span>scicon</span></a> <a href="https://mstdn.social/tags/chemivere" class="mention hashtag" rel="tag">#<span>chemivere</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/totalsynthesis" class="mention hashtag" rel="tag">#<span>totalsynthesis</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/lab" class="mention hashtag" rel="tag">#<span>lab</span></a> <a href="https://mstdn.social/tags/science" class="mention hashtag" rel="tag">#<span>science</span></a></p>
ChemistryViews<p>Synthesis of Bis-Benzofulvenes: Route from gem-dibromoolefins via bromobenzofulvene intermediates </p><p><a href="https://bit.ly/3MMApcr" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">bit.ly/3MMApcr</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/organic" class="mention hashtag" rel="tag">#<span>organic</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/scicon" class="mention hashtag" rel="tag">#<span>scicon</span></a></p>
ChemistryViews<p>Formal Cross-Coupling of Amines and Carboxylic Acids: Building blocks activated as pyridinium salts and N-acyl-glutarimides for C(sp3)–C(sp2) coupling </p><p><a href="https://bit.ly/3By8uqs" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">bit.ly/3By8uqs</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/science" class="mention hashtag" rel="tag">#<span>science</span></a> <a href="https://mstdn.social/tags/amines" class="mention hashtag" rel="tag">#<span>amines</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a></p>
ChemistryViews<p>🔬<a href="https://mstdn.social/tags/OnThisDay" class="mention hashtag" rel="tag">#<span>OnThisDay</span></a>, we remember Tetsuo Nozoe (born May 16, 1902 in Sendai, Japan), an exceptional organic chemist and autograph collector🧪📚 <br />Besides his work on non-benzoid aromatic rings, he is known for the discovery of hinokitiol (β-thujaplicin)</p><p><a href="https://www.chemistryviews.org/details/ezine/2222391/Tetsuo_Nozoe_Organic_Chemist_and_Autograph_Collector/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/details/ezi</span><span class="invisible">ne/2222391/Tetsuo_Nozoe_Organic_Chemist_and_Autograph_Collector/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/science" class="mention hashtag" rel="tag">#<span>science</span></a> <a href="https://mstdn.social/tags/scientist" class="mention hashtag" rel="tag">#<span>scientist</span></a> <a href="https://mstdn.social/tags/chemist" class="mention hashtag" rel="tag">#<span>chemist</span></a> <a href="https://mstdn.social/tags/organicsynthesis" class="mention hashtag" rel="tag">#<span>organicsynthesis</span></a></p>
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