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The Lautens Group
@thelautensgroup
šØš¦ Investigating and developing novel transition-metal-catalyzed organic transformations. insta: @theorderoflautens
ID: 1028767308301225984
https://www.chem.utoronto.ca/staff/ML/index.php 12-08-2018 22:16:54
1,1K Tweet
4,4K Followers
757 Following
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Way to go ā¦Bijan Mirabiā© on a Silver Medal poster at OMCOS. You did the ā¦The Lautens Groupā© proud yet again.

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We are delighted to welcome Dr. Alexa Torelli Alexa Torelli to @WWU_Muenster as an Humboldt-Stiftung post-doctoral research fellow! Alexa joins us from The Lautens Group, Mark Lautens OC at University of Toronto. Great to have you with us Alexa!

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Itās a wrap. PhDone for Dr Bijan Mirabi ā¦Bijan Mirabiā© #57 Heading off to a top job in industry straight from his degree. He did it all, synthesis, computation, medicinal chemistry with ā¦Structural Genomics Consortium (SGC)ā© catalysis, methodology and mechanism. Sad to see you go.

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You know what they say, āyou canāt trust a chemist who canāt cook.ā Good thing Bijan Mirabi is amazing at both. Thank you for the lunch today!

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Nickel-Catalyzed Reductive Alkyne Hydrocyanation Enabled by Malononitrile and a Formaldehyde Additive | Journal of the American Chemical Society University of Toronto Chemistry at UofT Total Synthesis and Methodology Highlights #Ni #Catalysis #Alkyne #Hydrocyanation #Malononitrile #Formaldehyde #Additive pubs.acs.org/doi/10.1021/jaā¦
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āļø In this Synfact of the month Mark Lautens OC (The Lautens Group) from University of Toronto highlighted the Ā“Rhodium Catalyzed Aryl CāH Functionalization with Nitroalkenes` by You S.-L. and co-workers from Shanghai Institute of Organic Chemistry.š§ š brnw.ch/21wEoh2
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š brnw.ch/21wEoh2 āļø In this Synfact of the month <a href="/MarkLautens/">Mark Lautens OC</a> (<a href="/TheLautensGroup/">The Lautens Group</a>) from <a href="/UofT/">University of Toronto</a> highlighted the Ā“Rhodium Catalyzed Aryl CāH Functionalization with Nitroalkenes` by You S.-L. and co-workers from Shanghai Institute of Organic Chemistry.š§
š brnw.ch/21wEoh2"
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Just out in #OrgLett, The Lautens Group reports the synthesis of enantioenriched spirocyclic Ī²-lactam pyrrolidinones in a copper-catalyzed Kinugasa/aldol domino reaction. Check it out here: pubs.acs.org/doi/10.1021/acā¦ Alexa Torelli, Mark Lautens OC

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Check out our latest paper in J Org Chem/Org Lett to Synthesize Enantioenriched Spirocyclic Ī²-Lactams. Congratulations to Alexa Torelli, Eun Seo, AurĆ©lien and Marcel. pubs.acs.org/doi/10.1021/acā¦
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Check out our latest paper in J. Am. Chem. Soc. to access bis-heterocycles via palladium catalysis. A great collaboration with Alan Aspuru-Guzik to study the photophysical properties. Congratulations to Ramon Arora, Bijan Mirabi, Andrew Durant, Carlota, and Austin. pubs.acs.org/doi/10.1021/jaā¦
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Palladium-Catalyzed Synthesis of Linked Bis-HeterocyclesāSynthesis and Investigation of Photophysical Properties | Journal of the American Chemical Society Mark Lautens OC University of Toronto Total Synthesis and Methodology Highlights #Pd #Catalysis #Heterocycles #Photophysical #Properties pubs.acs.org/doi/10.1021/jaā¦
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If you are interested in C(sp3)-H activation with Nickel, check out our latest review in #Synlett. A special issue dedicated to Keith Fagnou, written by Colton Johnson, Shangyu Li, Ramon Arora, Bijan Mirabi and Mark Lautens OC. thieme-connect.com/products/ejourā¦
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Check out our latest paper to make unsymmetrical linked bis-heterocycles using palladium domino catalysis. Congratulations to Ramon Arora , Jonathan Bajohr and Mark Lautens OC. pubs.acs.org/doi/10.1021/acā¦
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The group has been busy, even as I learn the job of Chair Chemistry at UofT Ramon Arora and Jon Bajohr put this work together - combining two of our favorite reactions. Some very sweet heterocycles.
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Check out our latest paper in ACS Catalysis! Here we report a nickel/visible light catalyzed carbohalogenation of aryl iodides and aryl bromides. Congratulations to Ramon Arora and Mark Lautens OC. pubs.acs.org/doi/10.1021/acā¦
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While in the past solo efforts were common in the group, they have become less frequent in recent years since we host many visitors from abroad, and they often pair up and share authorship. This effort by Ramon Arora is a throwback to those earlier days. Congratulations x1
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Check out our latest paper in Chemistry at Thieme Synthesis! Here we report a Base-mediated synthesis of 2-bromo benzoheterocycles. Congratulations to Ramon Arora Shangyu Li, Maik Stommer, Bijan Mirabi and Mark Lautens OC thieme-connect.com/products/ejourā¦ š·