Organic Chemistry Portal
@organicportal.bsky.social
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The Organic Chemistry Portal - For daily updates please visit https://www.organic-chemistry.org/abstracts/ and check out https://www.organic-chemistry.org/info/linking/
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organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
A decarboxylative cyanomethylation of β-aryl/heteroaryl substituted α,β-unsaturated carboxylic acids
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
Use of a nickel catalyst in combination with a photoredox catalyst and light leads to much more active alkylation catalysts
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
Visible-light-induced singlet nucleophilic carbene intermediates can be trapped by fluorinated ketones via 1,2-carbonyl addition
organicportal.bsky.social
The video of the announcement: www.youtube.com/watch?v=0d02... For more information, please also check out our other posts here. And I'm sure we'll cover some catalytically active MOFs in the future as part of our project.
organicportal.bsky.social
For a concise introduction to the chemistry and design principles behind important metal-organic frameworks and related porous materials, we recommend the book authored by Omar M. Yaghi et al: Americas: amzn.to/4mYd5Y6 , EU: amzn.to/3VShKjp , UK: amzn.to/3KDDIUU
organicportal.bsky.social
Following the laureates’ groundbreaking discoveries, chemists have built tens of thousands of different MOFs. Some of these may contribute to solving some of humankind’s greatest challenges, with applications that include...
Nobel Prize in Chemistry 2025
The Nobel Prize in Chemistry 2025 was awarded to Susumu Kitagawa, Richard Robson and Omar M. Yaghi “for the development of metal-organic frameworks.”
www.nobelprize.org
organicportal.bsky.social
Metal-organic frameworks have enormous potential, bringing previously unforeseen opportunities for custom-made materials with new functions,” says Heiner Linke, Chair of the Nobel Committee for Chemistry.
organicportal.bsky.social
The Nobel Prize in Chemistry has just been awarded to Susumu Kitagawa, Kyoto University, Japan; Richard Robson, University of Melbourne, Australia and Omar M. Yaghi, University of California, Berkeley, USA for "the development of metal-organic frameworks. www.nobelprize.org/prizes/chemi...
organicportal.bsky.social
So yes, just the new contributions will be paywalled. And if you if need to access the information: inform your librarian. The rate schedule for universities will be very fair. It's a cheap set-up fee (a single payment). I will even take very fair rates from companies. However, things must change.
organicportal.bsky.social
So everyone, who now tells me, that he/she leaves: I am fine with your decisions. Without paywalling, there won't be any updates anyway in 2026. And whether I paywall new contributions or just don't publish them, does not make a difference.
organicportal.bsky.social
TBH there is a reason, why sites like Synarchive or organic-reaction.com are +/- dead. The question is not, whether people leave, the question is, whether I have the opportunity to increase the usefulness of the website or not. And currently (AI, hosting fees etc, share of donations), I must say no.
organicportal.bsky.social
OK, I now clearly write, that the paywalled DH has aprox. 1/20 of the visitors we have but can finance more than 12 co-workers, while our ad income hardly finances one. Because people don't click or have ads blocked. And companies run ads via google. Do you see the problem or a solution?
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
A decarboxylative cyanomethylation of β-aryl/heteroaryl substituted α,β-unsaturated carboxylic acids
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
Use of a nickel catalyst in combination with a photoredox catalyst and light leads to much more active alkylation catalysts for the synthesis of tertiary nitroalkanes
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
Visible-light-induced singlet nucleophilic carbene intermediates can be trapped by fluorinated ketones via 1,2-carbonyl addition
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
An efficient reaction of o-acylanilines with α-hydroxyketones provides 3-hydroxyquinolines in good yields.
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
A copper-catalyzed hydrodechlorination of primary, secondary, and tertiary alkyl chlorides using diisobutylaluminum hydride
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
An operationally simple and scalable Cu-catalyzed asymmetric conjugate addition of trialkenylboroxines to enone diesters
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
Pharmaceutically important azolo[1,5-a]pyrimidines can be synthesized from widely available 3- or 5-aminoazoles, aldehydes, and triethylamine.
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
A photocatalytic three-component cascade reaction of readily available enaminones, hydrazines, and CBr4
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
Tetrahydropyranones are synthesized from 3-bromobut-3-en-1-ols and aldehydes in good yields with excellent diastereoselectivity
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
A rhodium-catalyzed intermolecular dehydrogenative Si-O coupling between dihydrosilanes and silanols or alcohols provides various highly functionalized chiral siloxanes and alkoxysilanes in decent yields with excellent stereocontrol.
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
Ca(NTf2)2 catalyzes a reaction of sulfonyl fluorides, fluorosulfates, and sulfamoyl fluorides with silyl amines into S-N bond-containing compounds
organicportal.bsky.social
www.organic-chemistry.org/abstracts/li...
A facile switchable regioselective 7-endo or 6-exo iodocyclization of O-homoallyl benzimidates