Eggs & segs?
Kraken & bacon?
Beans & diazepines?
Kraken & bacon?
Beans & diazepines?
June 29, 2026 at 10:22 PM
Eggs & segs?
Kraken & bacon?
Beans & diazepines?
Kraken & bacon?
Beans & diazepines?
When this big guy moved in with us, his name was Benzo.
I didn't like him being named after a drug (especially with the foster kiddos about), so I decided it was short for Benzamin.
Naturally, his middle name is Diazepines
I didn't like him being named after a drug (especially with the foster kiddos about), so I decided it was short for Benzamin.
Naturally, his middle name is Diazepines
January 8, 2025 at 5:34 PM
When this big guy moved in with us, his name was Benzo.
I didn't like him being named after a drug (especially with the foster kiddos about), so I decided it was short for Benzamin.
Naturally, his middle name is Diazepines
I didn't like him being named after a drug (especially with the foster kiddos about), so I decided it was short for Benzamin.
Naturally, his middle name is Diazepines
Rapid access to 1,2- #diazepines from #pyridines via ylide formation under 370 nm light, as reported in the paper of Tomislav Rovis & coworkers🚀 Tuning the protecting group enables diverse substrates, offering a one-pot route to rare drug-like cores💊
👉 buff.ly/UXBkq9a
👉 buff.ly/UXBkq9a
October 24, 2025 at 7:02 AM
Rapid access to 1,2- #diazepines from #pyridines via ylide formation under 370 nm light, as reported in the paper of Tomislav Rovis & coworkers🚀 Tuning the protecting group enables diverse substrates, offering a one-pot route to rare drug-like cores💊
👉 buff.ly/UXBkq9a
👉 buff.ly/UXBkq9a
Out today in ChemRxiv, we report the synthesis of 1,2-diazepines-fused β-lactams under gentle photochemical activation. Commercially available 1-aminopyridinium iodide can be directly engaged in a one-pot sequence. KUDOS to Jules for his dedication to the project!
chemrxiv.org/engage/chemr...
chemrxiv.org/engage/chemr...
July 17, 2025 at 11:45 AM
Out today in ChemRxiv, we report the synthesis of 1,2-diazepines-fused β-lactams under gentle photochemical activation. Commercially available 1-aminopyridinium iodide can be directly engaged in a one-pot sequence. KUDOS to Jules for his dedication to the project!
chemrxiv.org/engage/chemr...
chemrxiv.org/engage/chemr...
and yet i have none 😔 the world is cruel and my diazepines un-benzo'd
June 25, 2024 at 12:28 AM
and yet i have none 😔 the world is cruel and my diazepines un-benzo'd
Gonna need some bezos-diazepines, amirite
May 5, 2026 at 1:43 AM
Gonna need some bezos-diazepines, amirite
This research presents a novel Tf2O-promoted [5+2] annulation strategy for the synthesis of 1,4-diazepines from imidazolidines and ynamides.
September 10, 2025 at 1:41 PM
This research presents a novel Tf2O-promoted [5+2] annulation strategy for the synthesis of 1,4-diazepines from imidazolidines and ynamides.
He had seven different drugs in him, including coke, amphetamines, diazepines. Apparently. He’s a doctor of psychotherapy. It’s all unfathomable.
December 21, 2024 at 10:28 AM
He had seven different drugs in him, including coke, amphetamines, diazepines. Apparently. He’s a doctor of psychotherapy. It’s all unfathomable.
🌟 One-pot photochemical method transforms pyridines into bicyclic pyrazolines, pyrazoles, or 1,2-diazepines
www.chemistryviews.org/using-light-...
www.chemistryviews.org/using-light-...
Using Light to Edit the Molecular Skeleton of Pyridines - ChemistryViews
Efficient one-pot photochemical method transforms pyridines into bicyclic pyrazolines, pyrazoles, or 1,2-diazepines
www.chemistryviews.org
June 17, 2024 at 12:55 PM
🌟 One-pot photochemical method transforms pyridines into bicyclic pyrazolines, pyrazoles, or 1,2-diazepines
www.chemistryviews.org/using-light-...
www.chemistryviews.org/using-light-...
Extract: The PhD thesis will be conducted in the Organic Synthesis group at the Institut Lavoisier de Versailles, focusing on enantioselective elaboration of diazepines using organo- and transition metal-catalysis.
September 12, 2026 at 5:27 PM
Extract: The PhD thesis will be conducted in the Organic Synthesis group at the Institut Lavoisier de Versailles, focusing on enantioselective elaboration of diazepines using organo- and transition metal-catalysis.
Cool to see more 1,2-diazepines! The intro does not really reflect the state of the art though 🤷♂️ anyway, at least we are cited…
Rapid access to 1,2- #diazepines from #pyridines via ylide formation under 370 nm light, as reported in the paper of Tomislav Rovis & coworkers🚀 Tuning the protecting group enables diverse substrates, offering a one-pot route to rare drug-like cores💊
👉 buff.ly/UXBkq9a
👉 buff.ly/UXBkq9a
October 25, 2025 at 10:50 AM
Cool to see more 1,2-diazepines! The intro does not really reflect the state of the art though 🤷♂️ anyway, at least we are cited…
You need to know first if you are allergic to opioids or benzo-diazepines, because that's what they use when you get there.
August 12, 2025 at 5:46 PM
You need to know first if you are allergic to opioids or benzo-diazepines, because that's what they use when you get there.
Feed: "Nature Communications"
By: Armido Studer
By: Armido Studer
Formal pyridine meta-azidation and its application for the synthesis of diazepines, ring-fused δ-carbolines and 1,2,3-triazolylpyridines
Late-stage peripheral functionalization and structural editing of nitrogen-containing heterocycles have garnered increasing attention due to their potential for the preparation of diversifying drug-like libraries. Herein, the authors report a peripheral regioselective meta-azidation of pyridines through dearomatized oxazino pyridine intermediates, and a subsequent molecular editing step via a photo-mediated singlet nitrene insertion process.
www.nature.com
October 24, 2025 at 4:18 AM
Feed: "Nature Communications"
By: Armido Studer
By: Armido Studer
Seems like every day is a battle over how many diazepines to take
August 9, 2025 at 1:07 AM
Seems like every day is a battle over how many diazepines to take
Discover a groundbreaking [5+2] annulation that unlocks the efficient synthesis of diverse 1,4-diazepines, a key class of N-heterocycles, through a simple, eco-friendly, and atom-economic...
🧵 Thread below
Full analysis: https://helixbrief.com/article/ee36a007-480f-409e-80c8-0b66cc91fb53
🧵 Thread below
Full analysis: https://helixbrief.com/article/ee36a007-480f-409e-80c8-0b66cc91fb53
September 10, 2025 at 1:41 PM
Discover a groundbreaking [5+2] annulation that unlocks the efficient synthesis of diverse 1,4-diazepines, a key class of N-heterocycles, through a simple, eco-friendly, and atom-economic...
🧵 Thread below
Full analysis: https://helixbrief.com/article/ee36a007-480f-409e-80c8-0b66cc91fb53
🧵 Thread below
Full analysis: https://helixbrief.com/article/ee36a007-480f-409e-80c8-0b66cc91fb53