Congratulations to Brandon Wright , Alessio Regni ,and Nattawadee Chaisan on the beautiful synthesis of daphenylline in JACS.  pubs.acs.org/doi/epdf/10.10…

Triaryl boranes: Where science takes a playful turn! 🙃🙂🙃Our latest research sheds light on the exotic molecular behavior of single-centered, multiple Lewis acidity. Discover our paper, now available as a preprint: go.shr.lc/3SwVFWH

It’s out! Check our nature publication about charge relocation! nature.com/articles/s4158… Congratulations to the team! #Bogdan Giulia Iannelli Daniel Kaiser #oxacarbeniumgang

Check out our group’s first review article-- a minireview describing how you can get to diverse cation synthons using alkene thianthrenation electrophiles! It’s been amazing to see the progress in this area! bit.ly/3usdcGc

Natural Product Synthesis in the 21st Century: Beyond the Mountain Top | ACS Central Science pubs.acs.org/doi/10.1021/ac… Inspiring read!

Oxygen is enough!! And it works great for the synthesis of 12 natural products!! Many congrats to Kiki Gennaiou and Antonis Kelesidis! Climbing the Oxidase Phase Ladder by Using Dioxygen as the Sole Oxidant: The Case Study of Costunolide | Organic Letters pubs.acs.org/doi/10.1021/ac…

A few years ago, we uncovered an unusual Z-selective allylic functionalization. We had no idea whatsoever how it worked. Karina and Achyut Ranjan Gogoi teamed up to map out the full mechanism and identify the origin of stereoinduction!! Check out our first detailed mechanism paper!

Building upon the inspiration from yesterday's talk during his visit to Budapest, today's highlight was the chance to connect with Ben Feringa from Feringa Lab and delve into intriguing scientific discussions with fellow group members. His insights are deeply appreciated!

Happy to share our work on bioinspired meroterpenoids synthesized in the The Magauer Lab that induce a lipid mediator class switch to inflammation resolution, available now as preprint: biorxiv.org/cgi/content/sh… #inflammation #oxylipin #lipidomics #lipoxygenase #proresolving

In this paper, 3rd year graduate student 李春雨 (Chunyu Li) synthesized 25 natural products (!!) using a method of in silico library selection. Chunyu is a new type of student in our lab, having seamlessly blended calculation and synthesis. Take a look: tinyurl.com/mryjxh2w

Direct olefin difunctionalization using anomeric amides, without catalysts & additives! The products, MultiFunctional HydroxylAmines (MFHAs), are building blocks for the synthesis of complex amines. Kudos to Young-Do Young Do Kwon & Daniel Daniel Joaquin! chemrxiv.org/engage/chemrxi…

Here we introduce the concept of a "structural pin," a hydrogen bond that predominantly dictates the conformation of a macrocycle. This discovery offers a tool for examining the dynamic behavior of macrocycles and optimizing their structures. Angewandte Chemie onlinelibrary.wiley.com/doi/10.1002/an…

Interested in alkaloid total synthesis, strained heterocycles, or metathesis? Find Krisz and Szilárd at the #BOSS_symposium (P007, P286) and explore our latest research findings!😉😀 #BOSSXVIII

A tribute to Katritzky chemistry: we're excited to share how benzotriazole aids in amide bioisostere construction onlinelibrary.wiley.com/doi/10.1002/an… Mykhailiuk Chem 🇺🇦 Angewandte Chemie

We are happy to share our joint paper with Prof. Tibor Soós (Soos OrgCat Lab): "Strain-Release-Driven Modular Synthesis of Oxetane-Based Amide Bioisosteres: Concise, Robust and Scalable Approach," co-authored by Enamine scientists: ‌Yarema Galushchak and ‌Pavel Mykhailiuk

Excited to share our newest strategy to access carbenes from aldehydes - now via radicals! Young & Jake found this highly practical, efficient, & selective way to make triangles - that even works in the presence of air or water! J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…

We are pleased to share one of our fun projects that illuminates the existence of a peculiar phenomenon: single-centered but multiple Lewis acidity: pubs.rsc.org/en/content/art…