Published by @rsc.org 🌐 Website: rsc.li/orgchemfront
𝐉𝐚𝐧𝐮𝐬-𝐭𝐲𝐩𝐞 𝐩𝐡𝐨𝐭𝐨-𝐫𝐞𝐝𝐨𝐱 𝐩𝐫𝐨𝐩𝐞𝐫𝐭𝐢𝐞𝐬 𝐚𝐧𝐝 𝐜𝐚𝐭𝐚𝐥𝐲𝐭𝐢𝐜 𝐚𝐩𝐩𝐥𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬 𝐨𝐟 𝟓,𝟏𝟎-𝐝𝐢𝐡𝐲𝐝𝐫𝐨𝐩𝐡𝐞𝐧𝐚𝐳𝐢𝐧𝐞 𝐝𝐞𝐫𝐢𝐯𝐚𝐭𝐢𝐯𝐞𝐬
🔗 doi.org/10.1039/D5QO01348H
𝐉𝐚𝐧𝐮𝐬-𝐭𝐲𝐩𝐞 𝐩𝐡𝐨𝐭𝐨-𝐫𝐞𝐝𝐨𝐱 𝐩𝐫𝐨𝐩𝐞𝐫𝐭𝐢𝐞𝐬 𝐚𝐧𝐝 𝐜𝐚𝐭𝐚𝐥𝐲𝐭𝐢𝐜 𝐚𝐩𝐩𝐥𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬 𝐨𝐟 𝟓,𝟏𝟎-𝐝𝐢𝐡𝐲𝐝𝐫𝐨𝐩𝐡𝐞𝐧𝐚𝐳𝐢𝐧𝐞 𝐝𝐞𝐫𝐢𝐯𝐚𝐭𝐢𝐯𝐞𝐬
🔗 doi.org/10.1039/D5QO01348H
𝐏𝐝-𝐜𝐚𝐭𝐚𝐥𝐲𝐬𝐞𝐝 𝐟𝐥𝐨𝐰 𝐓𝐬𝐮𝐣𝐢–𝐓𝐫𝐨𝐬𝐭 𝐚𝐥𝐥𝐲𝐥𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 𝐩𝐡𝐞𝐧𝐨𝐥𝐬: 𝐜𝐨𝐧𝐭𝐢𝐧𝐮𝐨𝐮𝐬-𝐟𝐥𝐨𝐰, 𝐞𝐱𝐭𝐫𝐚𝐜𝐭𝐢𝐨𝐧-𝐟𝐫𝐞𝐞 𝐬𝐲𝐧𝐭𝐡𝐞𝐬𝐢𝐬 𝐨𝐟 𝐞𝐬𝐦𝐨𝐥𝐨𝐥 𝐯𝐢𝐚 𝐚𝐥𝐥𝐲𝐥𝐚𝐭𝐢𝐨𝐧, 𝐞𝐩𝐨𝐱𝐢𝐝𝐚𝐭𝐢𝐨𝐧, 𝐚𝐧𝐝 𝐚𝐦𝐢𝐧𝐨𝐥𝐲𝐬𝐢𝐬 by Shū Kobayashi 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO01336D
𝐏𝐝-𝐜𝐚𝐭𝐚𝐥𝐲𝐬𝐞𝐝 𝐟𝐥𝐨𝐰 𝐓𝐬𝐮𝐣𝐢–𝐓𝐫𝐨𝐬𝐭 𝐚𝐥𝐥𝐲𝐥𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 𝐩𝐡𝐞𝐧𝐨𝐥𝐬: 𝐜𝐨𝐧𝐭𝐢𝐧𝐮𝐨𝐮𝐬-𝐟𝐥𝐨𝐰, 𝐞𝐱𝐭𝐫𝐚𝐜𝐭𝐢𝐨𝐧-𝐟𝐫𝐞𝐞 𝐬𝐲𝐧𝐭𝐡𝐞𝐬𝐢𝐬 𝐨𝐟 𝐞𝐬𝐦𝐨𝐥𝐨𝐥 𝐯𝐢𝐚 𝐚𝐥𝐥𝐲𝐥𝐚𝐭𝐢𝐨𝐧, 𝐞𝐩𝐨𝐱𝐢𝐝𝐚𝐭𝐢𝐨𝐧, 𝐚𝐧𝐝 𝐚𝐦𝐢𝐧𝐨𝐥𝐲𝐬𝐢𝐬 by Shū Kobayashi 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO01336D
🔗 doi.org/10.1039/D5QO01123J
🔗 doi.org/10.1039/D5QO01123J
𝐒𝐮𝐛-𝐫𝐨𝐨𝐦 𝐭𝐞𝐦𝐩𝐞𝐫𝐚𝐭𝐮𝐫𝐞 𝐭𝐫𝐚𝐧𝐬𝐟𝐞𝐫 𝐡𝐲𝐝𝐫𝐨𝐠𝐞𝐧𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 α,β-𝐮𝐧𝐬𝐚𝐭𝐮𝐫𝐚𝐭𝐞𝐝 𝐤𝐞𝐭𝐨𝐧𝐞𝐬 𝐮𝐬𝐢𝐧𝐠 𝐦𝐞𝐭𝐡𝐚𝐧𝐨𝐥 𝐚𝐬 𝐚 𝐡𝐲𝐝𝐫𝐨𝐠𝐞𝐧 𝐬𝐨𝐮𝐫𝐜𝐞 by Sanjay Pratihar 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO01133G
𝐒𝐮𝐛-𝐫𝐨𝐨𝐦 𝐭𝐞𝐦𝐩𝐞𝐫𝐚𝐭𝐮𝐫𝐞 𝐭𝐫𝐚𝐧𝐬𝐟𝐞𝐫 𝐡𝐲𝐝𝐫𝐨𝐠𝐞𝐧𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 α,β-𝐮𝐧𝐬𝐚𝐭𝐮𝐫𝐚𝐭𝐞𝐝 𝐤𝐞𝐭𝐨𝐧𝐞𝐬 𝐮𝐬𝐢𝐧𝐠 𝐦𝐞𝐭𝐡𝐚𝐧𝐨𝐥 𝐚𝐬 𝐚 𝐡𝐲𝐝𝐫𝐨𝐠𝐞𝐧 𝐬𝐨𝐮𝐫𝐜𝐞 by Sanjay Pratihar 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO01133G
@feringalab.bsky.social & Nazario Martin.
Detailed information could be found here:
🔗 www.rsc.org/publishing/j...
@feringalab.bsky.social & Nazario Martin.
Detailed information could be found here:
🔗 www.rsc.org/publishing/j...
𝐒𝐢𝐭𝐞 𝐬𝐞𝐥𝐞𝐜𝐭𝐢𝐯𝐞 𝐇𝐞𝐜𝐤 𝐚𝐫𝐲𝐥𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 𝐍-𝐯𝐢𝐧𝐲𝐥-𝟕-𝐚𝐳𝐚𝐢𝐧𝐝𝐨𝐥𝐞 𝐞𝐧𝐠𝐢𝐧𝐞𝐞𝐫𝐞𝐝 𝐛𝐲 𝐍-𝐨𝐱𝐢𝐝𝐞 𝐚𝐜𝐭𝐢𝐯𝐚𝐭𝐢𝐨𝐧: 𝐬𝐜𝐨𝐩𝐞 𝐚𝐧𝐝 𝐦𝐞𝐜𝐡𝐚𝐧𝐢𝐬𝐭𝐢𝐜 𝐬𝐭𝐮𝐝𝐢𝐞𝐬
by Parthasarathi Das 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO00976F
𝐒𝐢𝐭𝐞 𝐬𝐞𝐥𝐞𝐜𝐭𝐢𝐯𝐞 𝐇𝐞𝐜𝐤 𝐚𝐫𝐲𝐥𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 𝐍-𝐯𝐢𝐧𝐲𝐥-𝟕-𝐚𝐳𝐚𝐢𝐧𝐝𝐨𝐥𝐞 𝐞𝐧𝐠𝐢𝐧𝐞𝐞𝐫𝐞𝐝 𝐛𝐲 𝐍-𝐨𝐱𝐢𝐝𝐞 𝐚𝐜𝐭𝐢𝐯𝐚𝐭𝐢𝐨𝐧: 𝐬𝐜𝐨𝐩𝐞 𝐚𝐧𝐝 𝐦𝐞𝐜𝐡𝐚𝐧𝐢𝐬𝐭𝐢𝐜 𝐬𝐭𝐮𝐝𝐢𝐞𝐬
by Parthasarathi Das 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO00976F
𝐁𝐲𝐩𝐚𝐬𝐬𝐢𝐧𝐠 𝐭𝐡𝐞 𝐚𝐛𝐧𝐨𝐫𝐦𝐚𝐥 𝐂𝐡𝐢𝐜𝐡𝐢𝐛𝐚𝐛𝐢𝐧 𝐫𝐞𝐚𝐜𝐭𝐢𝐨𝐧 𝐝𝐞𝐚𝐝-𝐞𝐧𝐝 𝐩𝐫𝐨𝐯𝐢𝐝𝐞𝐬 𝐚 𝐛𝐢𝐨𝐦𝐢𝐦𝐞𝐭𝐢𝐜 𝐚𝐜𝐜𝐞𝐬𝐬 𝐭𝐨 𝐩𝐫𝐞-𝐡𝐚𝐨𝐮𝐚𝐦𝐢𝐧𝐞
by Mehdi A. Beniddir, Erwan Poupon 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO01111F
𝐁𝐲𝐩𝐚𝐬𝐬𝐢𝐧𝐠 𝐭𝐡𝐞 𝐚𝐛𝐧𝐨𝐫𝐦𝐚𝐥 𝐂𝐡𝐢𝐜𝐡𝐢𝐛𝐚𝐛𝐢𝐧 𝐫𝐞𝐚𝐜𝐭𝐢𝐨𝐧 𝐝𝐞𝐚𝐝-𝐞𝐧𝐝 𝐩𝐫𝐨𝐯𝐢𝐝𝐞𝐬 𝐚 𝐛𝐢𝐨𝐦𝐢𝐦𝐞𝐭𝐢𝐜 𝐚𝐜𝐜𝐞𝐬𝐬 𝐭𝐨 𝐩𝐫𝐞-𝐡𝐚𝐨𝐮𝐚𝐦𝐢𝐧𝐞
by Mehdi A. Beniddir, Erwan Poupon 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO01111F
𝐄𝐥𝐞𝐜𝐭𝐫𝐨𝐩𝐡𝐢𝐥𝐢𝐜 𝐢𝐧𝐬𝐞𝐫𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐫𝐢𝐧𝐠 𝐠𝐫𝐨𝐰𝐭𝐡 𝐢𝐧 𝟏,𝟐,𝟓-𝐚𝐳𝐚𝐝𝐢𝐛𝐨𝐫𝐨𝐥𝐢𝐝𝐢𝐧𝐞𝐬: 𝐭𝐡𝐞𝐨𝐫𝐞𝐭𝐢𝐜𝐚𝐥 𝐞𝐯𝐢𝐝𝐞𝐧𝐜𝐞 𝐟𝐨𝐫 𝐛𝐨𝐫𝐨𝐧-𝐝𝐫𝐢𝐯𝐞𝐧 𝐞𝐱𝐩𝐚𝐧𝐬𝐢𝐨𝐧
by J. Oscar C. Jiménez-Halla 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO...
𝐄𝐥𝐞𝐜𝐭𝐫𝐨𝐩𝐡𝐢𝐥𝐢𝐜 𝐢𝐧𝐬𝐞𝐫𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐫𝐢𝐧𝐠 𝐠𝐫𝐨𝐰𝐭𝐡 𝐢𝐧 𝟏,𝟐,𝟓-𝐚𝐳𝐚𝐝𝐢𝐛𝐨𝐫𝐨𝐥𝐢𝐝𝐢𝐧𝐞𝐬: 𝐭𝐡𝐞𝐨𝐫𝐞𝐭𝐢𝐜𝐚𝐥 𝐞𝐯𝐢𝐝𝐞𝐧𝐜𝐞 𝐟𝐨𝐫 𝐛𝐨𝐫𝐨𝐧-𝐝𝐫𝐢𝐯𝐞𝐧 𝐞𝐱𝐩𝐚𝐧𝐬𝐢𝐨𝐧
by J. Oscar C. Jiménez-Halla 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO...
𝐂𝐨𝐨𝐩𝐞𝐫𝐚𝐭𝐢𝐯𝐞 𝐍-𝐡𝐞𝐭𝐞𝐫𝐨𝐜𝐲𝐜𝐥𝐢𝐜 𝐜𝐚𝐫𝐛𝐞𝐧𝐞/𝐩𝐡𝐨𝐭𝐨𝐜𝐚𝐭𝐚𝐥𝐲𝐬𝐢𝐬: 𝐯𝐢𝐬𝐢𝐛𝐥𝐞-𝐥𝐢𝐠𝐡𝐭-𝐩𝐫𝐨𝐦𝐨𝐭𝐞𝐝 𝐭𝐚𝐧𝐝𝐞𝐦 α-𝐬𝐩³ 𝐂–𝐇 𝐚𝐜𝐭𝐢𝐯𝐚𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐫𝐞𝐝𝐮𝐜𝐭𝐢𝐯𝐞 𝐍-𝐚𝐥𝐤𝐲𝐥𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 𝐭𝐞𝐭𝐫𝐚𝐡𝐲𝐝𝐫𝐨𝐢𝐬𝐨𝐪𝐮𝐢𝐧𝐨𝐥𝐢𝐧𝐞
by C. Uma Maheswari 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO...
𝐂𝐨𝐨𝐩𝐞𝐫𝐚𝐭𝐢𝐯𝐞 𝐍-𝐡𝐞𝐭𝐞𝐫𝐨𝐜𝐲𝐜𝐥𝐢𝐜 𝐜𝐚𝐫𝐛𝐞𝐧𝐞/𝐩𝐡𝐨𝐭𝐨𝐜𝐚𝐭𝐚𝐥𝐲𝐬𝐢𝐬: 𝐯𝐢𝐬𝐢𝐛𝐥𝐞-𝐥𝐢𝐠𝐡𝐭-𝐩𝐫𝐨𝐦𝐨𝐭𝐞𝐝 𝐭𝐚𝐧𝐝𝐞𝐦 α-𝐬𝐩³ 𝐂–𝐇 𝐚𝐜𝐭𝐢𝐯𝐚𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐫𝐞𝐝𝐮𝐜𝐭𝐢𝐯𝐞 𝐍-𝐚𝐥𝐤𝐲𝐥𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 𝐭𝐞𝐭𝐫𝐚𝐡𝐲𝐝𝐫𝐨𝐢𝐬𝐨𝐪𝐮𝐢𝐧𝐨𝐥𝐢𝐧𝐞
by C. Uma Maheswari 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO...
𝐓𝐮𝐧𝐚𝐛𝐥𝐞 𝐭𝐡𝐢𝐨𝐟𝐮𝐦𝐚𝐫𝐚𝐭𝐞 𝐬𝐭𝐞𝐫𝐞𝐨𝐬𝐞𝐥𝐞𝐜𝐭𝐢𝐯𝐞 𝐜𝐲𝐜𝐥𝐨𝐚𝐝𝐝𝐢𝐭𝐢𝐨𝐧𝐬 𝐯𝐢𝐚 𝐚𝐦𝐢𝐧𝐨𝐦𝐞𝐟𝐥𝐨𝐪𝐮𝐢𝐧𝐞 𝐜𝐚𝐭𝐚𝐥𝐲𝐬𝐢𝐬
by Rafał Szabla, Rafał Kowalczyk 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO...
𝐓𝐮𝐧𝐚𝐛𝐥𝐞 𝐭𝐡𝐢𝐨𝐟𝐮𝐦𝐚𝐫𝐚𝐭𝐞 𝐬𝐭𝐞𝐫𝐞𝐨𝐬𝐞𝐥𝐞𝐜𝐭𝐢𝐯𝐞 𝐜𝐲𝐜𝐥𝐨𝐚𝐝𝐝𝐢𝐭𝐢𝐨𝐧𝐬 𝐯𝐢𝐚 𝐚𝐦𝐢𝐧𝐨𝐦𝐞𝐟𝐥𝐨𝐪𝐮𝐢𝐧𝐞 𝐜𝐚𝐭𝐚𝐥𝐲𝐬𝐢𝐬
by Rafał Szabla, Rafał Kowalczyk 𝘦𝘵 𝘢𝘭.
🔗 doi.org/10.1039/D5QO...
Oxidative copper-catalyzed synthesis of β-amino ketones from allyl alcohols and anilines
#Free_to_read
🔗 doi.org/10.1039/D5QO...
Oxidative copper-catalyzed synthesis of β-amino ketones from allyl alcohols and anilines
#Free_to_read
🔗 doi.org/10.1039/D5QO...
Exploring the intricacies of inverse hydride shuttle catalysis in azabicyclic scaffold construction with contiguous stereocenters by Vidya Avasare 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗https://doi.org/10.1039/D5QO00627A
Exploring the intricacies of inverse hydride shuttle catalysis in azabicyclic scaffold construction with contiguous stereocenters by Vidya Avasare 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗https://doi.org/10.1039/D5QO00627A
Countercation- and solvent-controlled selective borohydride hydrogenation of alkenes in diaryl enones
#Free_to_read
🔗 doi.org/10.1039/D5QO...
Countercation- and solvent-controlled selective borohydride hydrogenation of alkenes in diaryl enones
#Free_to_read
🔗 doi.org/10.1039/D5QO...
Metal- and base-free spirocyclization of alkylidene oxindoles via photo- and mechanochemically-generated nitrile ylides and nitrile imines as 1,3-dipoles by Subhabrata Sen 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗DOI doi.org/10.1039/D5QO...
Metal- and base-free spirocyclization of alkylidene oxindoles via photo- and mechanochemically-generated nitrile ylides and nitrile imines as 1,3-dipoles by Subhabrata Sen 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗DOI doi.org/10.1039/D5QO...
⚡ Efficient 3+2 cycloadditions
⚡ Access to spiro[pyrrolidine-oxindoles] & spiro[indoline-pyrazolones]
doi.org/10.1039/D5QO00851D
#OrganicChemistry
⚡ Efficient 3+2 cycloadditions
⚡ Access to spiro[pyrrolidine-oxindoles] & spiro[indoline-pyrazolones]
doi.org/10.1039/D5QO00851D
#OrganicChemistry
Explore the latest research and insights in our newest issue — don’t miss it!
Explore the latest research and insights in our newest issue — don’t miss it!
Azlactone rings: uniting tradition and innovation in synthesis by Pedro P. de Castro, Giovanni W. Amarante 𝘦𝘵 𝘢𝘭.
#Free_to_read
doi.org/10.1039/D5QO...
Azlactone rings: uniting tradition and innovation in synthesis by Pedro P. de Castro, Giovanni W. Amarante 𝘦𝘵 𝘢𝘭.
#Free_to_read
doi.org/10.1039/D5QO...
👉 C–H bond halogenation: unlocking regiodivergence and enhancing selectivity through directing group strategies by Kamaldeep Paul et al.
🔗 doi.org/10.1039/D5QO00372E
👉 C–H bond halogenation: unlocking regiodivergence and enhancing selectivity through directing group strategies by Kamaldeep Paul et al.
🔗 doi.org/10.1039/D5QO00372E
Oxetane as a part of modern medicinal chemistry toolbox: the advanced synthesis of 3,3-disubstituted building blocks
#Free_to_read
🔗 doi.org/10.1039/D5QO...
Oxetane as a part of modern medicinal chemistry toolbox: the advanced synthesis of 3,3-disubstituted building blocks
#Free_to_read
🔗 doi.org/10.1039/D5QO...
"Direct Suzuki–Miyaura cross-coupling of C(sp²)–B(dan) bonds: designed in pursuit of usability" by Teruhisa Tsuchimoto 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗 doi.org/10.1039/D5QO...
"Direct Suzuki–Miyaura cross-coupling of C(sp²)–B(dan) bonds: designed in pursuit of usability" by Teruhisa Tsuchimoto 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗 doi.org/10.1039/D5QO...
"Garynthone A–I, PPAPs with diverse skeletons isolated from 𝘎𝘢𝘳𝘤𝘪𝘯𝘪𝘢 𝘺𝘶𝘯𝘯𝘢𝘯𝘦𝘯𝘴𝘪𝘴 and their immunosuppressive activity" by Jingming Jia, Anhua Wang 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗https://doi.org/10.1039/D5QO00414D
"Garynthone A–I, PPAPs with diverse skeletons isolated from 𝘎𝘢𝘳𝘤𝘪𝘯𝘪𝘢 𝘺𝘶𝘯𝘯𝘢𝘯𝘦𝘯𝘴𝘪𝘴 and their immunosuppressive activity" by Jingming Jia, Anhua Wang 𝘦𝘵 𝘢𝘭.
#Free_to_read
🔗https://doi.org/10.1039/D5QO00414D
👉Read the full research here:
doi.org/10.1039/D5QO...
doi.org/10.1039/D5QO...
#OCF_cover #Chemsky
👉Read the full research here:
doi.org/10.1039/D5QO...
doi.org/10.1039/D5QO...
#OCF_cover #Chemsky
#Supramolecular catalysis in the dearomative Michael addition involving nitro-group-activated benzofurans
by Anna Skrzyńska, Łukasz Albrecht et al. from Lodz University of Technology
doi.org/10.1039/D5QO...
#Supramolecular catalysis in the dearomative Michael addition involving nitro-group-activated benzofurans
by Anna Skrzyńska, Łukasz Albrecht et al. from Lodz University of Technology
doi.org/10.1039/D5QO...
⏰Time: 7:00 am (UK time)
📅Date: May 30, 2025
👉Register the webinar here: rsc.zoom.us/webinar/regi...
@rsc.org #OCF
⏰Time: 7:00 am (UK time)
📅Date: May 30, 2025
👉Register the webinar here: rsc.zoom.us/webinar/regi...
@rsc.org #OCF
👉Unraveling the α-effect in α-fluorinated carbanionic nucleophiles: origins and synthetic implications
by Jimin Yang and Xiao-Song Xue
#Chemsky #OCF_cover
doi.org/10.1039/D5QO...
👉Unraveling the α-effect in α-fluorinated carbanionic nucleophiles: origins and synthetic implications
by Jimin Yang and Xiao-Song Xue
#Chemsky #OCF_cover
doi.org/10.1039/D5QO...