Interesting difference in turn preferences for methyl- and chloroalkene isosteres. Substituent-Dependent Turn Switching in RGGY Peptidomimetics Containing Alkene Dipeptide Isosteres | The Journal of Organic Chemistry https://t.co/7RcTWvTwZF
Thiols upcycle BCBs into druglike 3D scaffolds ⚡️⚡️⚡️Lewis Acid-Catalyzed (3+3) Annulation of Bicyclo[1.1.0]butanes with Mercaptoacetaldehyde: Access to 2-Thiabicyclo[3.1.1]heptanes | Organic Letters https://t.co/brTqm7ruKj
Featuring an aryne-furan Diels-Alder cycloaddition 🔄. Biomimetic Synthesis of Seven Halenaquinone Meroterpenoids | Journal of the American Chemical Society https://t.co/ZwHRGRAW2r
Our Tutorial Review on strain-release driven reactions of BCBs, recently published in @ChemSocRev has been Highlighted as the (inside) front cover of the latest issue.
Please see the review👉https://t.co/GAVQwJ9BHi
Kudos to @shiksha_deswal & @RCD07_IISC@iiscbangalore
For chemists who are not afraid to try something new, this is an exciting time to be in MedChem R&D ⚗️ Advanced Synthetic Methods in Modern Medicinal Chemistry | Journal of Medicinal Chemistry https://t.co/sDbdpurFmi
An interesting way to activate BCBs- this could prove to be useful in a plethora of applications ⚡️⚡️⚡️ Phosphine‐Catalyzed Strain‐Release Alkynylation of Bicyclo [1.1.0] Butanes - Wang - 2026 - Advanced Synthesis & Catalysis - Wiley Online Library https://t.co/ajVSjnUGZi
Our conidiogenone B total synthesis is hot off the press @J_A_C_S! Cheers! @jo5i3bee@EmoryChem
Seven-Step Total Synthesis of Conidiogenone B Enabled by Radical Cyclizations | Journal of the American Chemical Society https://t.co/lhu1HXhqJA
Nice synthetic and structural work! 👏 Isolation and First Total Synthesis of PM100618 and PM110049, Two Structurally Distinct Marine-Derived Anticancer Oxazole Derivatives | The Journal of Organic Chemistry https://t.co/DR46t1CEqu
Happy to share our first preprint @ChemRxiv Base-Mediated (4+3) Strain-Release Cycloaddition of Indoles BCBs. Congratulations to @SayantanKundu16@pragati_kisan Thank you, Satish and group, @cdriacademy for computational studies @IISER_BERHAMPUR | https://t.co/2iHEdtZFno
🦋Double strain, double impact 💥! A dual strain-release cascade builds azetidine–bicyclopentane frameworks packed with quaternary centers—turning ring strain into powerful 3D complexity ⚡
@JOC_OL@dturesh@iiserkol
https://t.co/s1kxbT1dQ3
📅Lutz Ackermann @aztul, Peter Gölitz, Dieter Kaufmann, and Oliver Reiser @chemieimalltag have organized an Armin de Meijere Memorial Symposium, “From Small Rings to Large Compounds” (program: https://t.co/lvRM6Z6AQ4), which will take place on May 22, 2026, at the University of Göttingen @uniGoettingen. Attendance is free for all, registration required (see program).
Armin de Meijere (https://t.co/p9RgMTUSzQ) was not only a highly respected, internationally renowned organic chemist, he was also a great supporter of the autobiography series “Lives in Chemistry” (https://t.co/DBaasuTW4p). Ryoji Noyori, for example, thanked him explicitly in his autobiography for a “careful reading of the manuscript” (https://t.co/4Zk8ctu8U8).
Delighted to be part of New Synthetic Trends in Heterocycles!!! https://t.co/gzqYFindqw ⚗️Regioselective synthesis of functionalized 1,4-benzothiazines via intramolecular SNArF and SNArH cyclizations - ScienceDirect https://t.co/AmZWPhSkyb
The work of @josh_wwu@TobiasMilzarek and Matt on the synthesis of CF3-cycloproprenes using hypervalent iodine reagents and Cu(III) complexes is now published in Org. Lett.
https://t.co/anDpRHLCAE