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We are also looking for a motivated postdoc researcher! We welcome candidates with expertise in organic synthesis OR experimental physical chemistry (e.g., stopped-flow, kinetic profiling, molecular spectroscopy, etc.) Please send applications to [email protected] RT appreciated

Enantioselective Potassium-Catalyzed Wittig Olefinations | Journal of the American Chemical Society Harvard University Harvard Chemistry Jacobsen Lab Total Synthesis and Methodology Highlights #Enantioselective #K #Catalyzed #Wittig #Olefination pubs.acs.org/doi/10.1021/ja…

📢We are recruiting ! Looking for a #PhDposition in organic synthesis / asymmetric catalysis ? Two fully-funded PhD positions ICMMO. Come study enantioselective cycloadditions with us !

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

Please check out our crinipellin synthesis J. Am. Chem. Soc. ! Special thanks to Tantillo Lab for the DFT calculations! Concise Total Syntheses of (−)-Crinipellins A and B Enabled by a Controlled Cargill Rearrangement | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/ja…

Congrats to Dylan and Stephen for their method to glycosylate cotylenol and access 14-3-3 protein-client molecular glues! tinyurl.com/2y45ck4n Donor linker design was aided by Stephen’s “autoDFT” and solved a common problem in terpenoid synthesis: contrasteric glycosylation.

We're very excited to introduce a new series of graphical highlights created by our Editorial Board member Samiran Deb that we'll start releasing on a regular basis! This is our first one, focusing on a contrasteric glycosylation from the Shenvi Lab! ChemRxiv

Check out our latest graphical highlight from Samiran Deb, featuring the Sarpong Group synthesis of baphicacanthcusine A! Read the full article here: Angewandte Chemie doi.org/10.1002/anie.2…

In #JOrgChem: How exceptions and paradoxes in chemical reactivity advance our understanding: Explore the trade-off between useful and correct and the value of a systematic framework for addressing anomalies. Qiu Group #OpenAccess go.acs.org/bAM

Today we have a new graphical highlight thanks to Samiran Deb featuring Stoltz Group synthesis of hypersampsone M recently published in J. Am. Chem. Soc.!! doi.org/10.1021/jacs.4… More posters like this available at synthesis-workshop.com

The symbolism and the meaning of this moment for all Indians is not to be spoken about—it is only to be imagined… CHAK DE INDIAAAAAAAAAA! #GukeshDing #WorldChampion

Our group's new pre-print! A fully deductive model describing global rate-driving force relationships. It is NOT statistical fitting, and differs significantly from previous conceptual models😉 Eduardo García-Padilla deserves the highest appreciation! | ChemRxiv - go.shr.lc/3Q3EQka

📢We are recruiting postdocs and PhDs (start date flexible) to work on enantioselective cycloadditions/synthesis of complex polycycles. To apply send a CV, cover letter, research summary (for postdoc), BSc/MSc grades (for PhD) and contact info for at least 2 references via email

Our work on Transforming 2D Azolium Salts to 3D Caged Tertiary Amines is now published in Chemical Science. We appreciate excellent review process. Thanks to #ANRF and #ERP project (IIT Madras) is acknowledged for fundings. pubs.rsc.org/en/content/art…

Empowering Diastereoselective Cyclopropanation of Unactivated Alkenes with Sulfur Ylides through Nucleopalladation | Journal of the American Chemical Society IIT Madras Total Synthesis and Methodology Highlights JAIN (Deemed-to-be University)_Officials pubs.acs.org/doi/10.1021/ja…

We present a previously unrecognized dimension: dispersion affects how sensitively reaction barriers respond to driving force changes. We got another intrinsic reactivity modulator in hand🔥How London Dispersion Affects Intrinsic Reactivity | ChemRxiv - go.shr.lc/3G2lv0N

Photochemically Enabled #TotalSyntheses of Stemoamide Alkaloids by Nicholas R. Akkawi and David A. Nicewicz Nicewicz Lab at UNC-Chapel Hill Chemistry in J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…

It is now in Chemistry World magazine (Royal Society of Chemistry). Cascade reaction brings a new dimension to amine synthesis: chemistryworld.com/news/cascade-r…