catalysis, reaction discovery, and samoyed sled racing @scrippsresearch. views our own.

La Jolla, San Diego
🎥 My graduate-level #Organometallics course is now live on @YouTube! #chemtwitter Designed for PhD chemists, this series covers history, mechanisms, catalysis, ligand design & more. Offered once every 2 years—check it out anytime! 📺 tinyurl.com/5n9bjx5d
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Ni(0) for the masses! Paper now online: bit.ly/3bNzzaL @angew_chem. DM your shipping address for a free sample of this precatalyst.
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The 2023 @ScrippsGradPrgm Organometallics Course is live. All course materials available on the web: englelab.com/organometallics… All lectures on @YouTube: piped.video/watch?v=65XmR_…
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Meet the new bench-stable Ni(0) toolkit. bit.ly/3rKvC0S
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7-coordinate, it's the new 6-coordinate. W(0) catalysis, unleashed for migratory alkene carbonylation. Led by @W0TangClan together w/ @pengliu_group. Today in @ChemRxiv: bit.ly/2PQTBe9.
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How much NaOMe is actually in that nice-looking bottle of solid 'NaOMe' on your bench? 🤔🧐 Hint: maybe not much. Read the details in our most recent @ChemRxiv pre-print w/ #BMSChemistry here: bit.ly/2ElbqMs. #RealTimeChem
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Huge congrats to Jin-Quan @YulabJin @scrippsresearch on his ACS Somorjai Award at #ACSSpring2022! Glad that we requested seatbelts in the conference room!
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Lucky 7⃣...coordinate! The final version of our alkene isomerization/carbonylation reaction via W(0)/W(II) catalysis is online @NatureChemistry. Led by @W0TangClan @ziyangnickqin in collaboration w/ @pengliu_group. rdcu.be/cOQl2
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One of the strangest reactions we've ever worked on is described today in @ChemRxiv, a redox-paired alkene addition process in which two useful products are produced within the same cycle. bit.ly/3VAb9Hu @NiHuiqi w/ @houk1000 @pengliu_group
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The team. The team. The team. 🙏🏻
Congratulations to Scripps Research's Prof. Keary Engle, who has received this year’s Catalysts Young Investigator Award. Keary is recognized for his accomplishments in #organometallic #chemistry, organic synthesis and #catalysis scripps.edu/news-and-events/… @MDPIOpenAccess @EngleLab
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What a great day to be @scrippsresearch (and to be up late writing a grant 😂). Barry becomes only the 2nd person in history to win the chemistry Nobel twice. Congrats to all laureates!
BREAKING NEWS: The Royal Swedish Academy of Sciences has decided to award the 2022 #NobelPrize in Chemistry to Carolyn R. Bertozzi, Morten Meldal and K. Barry Sharpless “for the development of click chemistry and bioorthogonal chemistry.”
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Pd(0) w/o the fuss... tinyurl.com/2e63jcy9 @HarryHe88239850, Wenzhuo, & #BMSChemistry
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Delighted to see the final version of this collaborative study out in @angew_chem, describing a robust & scalable e-chem ⚡️ method to Ni(0) w/ #BMSChemistry @BaranLabReads @Julien07. Thx to our fearless leader @CamZRub! tinyurl.com/mr2yyy8a
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What showed up under the tree last night? 👀🎁🎄@angew_chem: bit.ly/3Yse2No
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The final version of this study on the discovery and mechanistic elucidation of an unusual anti-cyclopropanation rxn is now online @J_A_C_S. A great collaboration w/ @pengliu_group, Piercey lab @PUEnergetics, and #PfizerChemistry led by @NiHuiqi. tinyurl.com/3hmpjp4k
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That’s amore… 💕 Our brand new @MBRAUNsolutions glovebox is online in time for the new crop of G1 students.
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A year later, we've learned a lesson learned by many others: mechanistic work w/ Ni is hard! 🛠️ Nevertheless, we've made some progress and now share an updated @ChemRxiv pre-print shedding🔦 on how this stereodivergent isomerization works. @Julien07 tinyurl.com/kysaup5e
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W(0)/W(II) redox catalysis for alkene isomerization/hydroboration, now online in @J_A_C_S. Fun transatlantic collaboration w/ @MartinLab_ICIQ led by @W0TangClan @TitoBraulio. PS - Don't mind our subliminal messaging: W(0)/W(II)... [WOW]^2 🤩🤩 bit.ly/3hen8t2
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The culmination of a long journey & the start of another. Our 1st report on alkene 1,2-difunctionalization via a transient directing group. 3 rxn components 2 stereocenters: C-F and C-C 1 resilient team led by @liu_zhonglin & Luke 🧢s off! @ChemRxiv bit.ly/3sdUnAu
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4+ years in the making: We’re excited to describe the first use of a chiral transient directing group in Heck-type alkene additions #JustAccepted @angew_chem. Nice work by Luke and the project team, and great as always collaborating with @pengliu_group. bit.ly/2Ut2OrS
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Is my bisphosphine ligand oxidizing? How is it happening? Does it matter? 🤔 If these questions keep you up at night 🛌, you're not alone! Happy to share 3+ years of learnings, led by G4 student Shenghua together w/ @DonnaBlackmond #BMSChemistry. tinyurl.com/vc8x9zhw
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After >3 years of effort, very excited to share a solution to an incredibly hard selectivity control problem, stereoinduction in intermolecular arylnickel migratory insertion. @omar__apolinar @TaehoKang6 @pengliu_group @stevewiz06 #BMSChemistry @ChemRxiv bit.ly/3A9OdHY
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The 2nd is by a massive team effort led by @omar__apolinar @TaehoKang6 & @0iTurki w/ #BMSChemistry @pengliu_group, describing the 1st enantioselective 3-component diarylation of unactivated alkenes under Ni catalysis, appearing in @J_A_C_S: bit.ly/3RWY4X7
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During the past year, the G4 students teamed up to write a 📖 chapter on π-bond difunctionalization for Comprehensive Organometallic Chemistry IV, online this week. Thanks to our fearless editor @ianatonks! @ELSchemistry bit.ly/3dbLBwO
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Tungsten is known for its use in hard material, but here it offers a soft touch. Kinetic olefin transposition without over isomerization. bit.ly/3XhHFj4 @ChemRxiv Brought to you by Team W: @W0TangClan @CamZRub @TitoBraulio
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W(0) adds its own unique twist to classical catalytic alkene hydroboration. Thrilled to collaborated with chain-parkour masters @MartinLab_ICIQ. Props to project leads @W0TangClan & @TitoBraulio. #TeamTungsten @ChemRxiv pre-print: bit.ly/2TUwCkY
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Delighted to share the final version our asymmetric Pd-catalyzed alkene 1,2-arylfluorination w/ transient directing group #JustAccepted @J_A_C_S. Key step on a long TDG quest! Bravo @liu_zhonglin & team. bit.ly/3fKb1Uf
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Second, if you're looking for ~20 years of metal-catalyzed directed C(sp3)-H activation in one stop, @Binzju @AndrewMRomine & @CamZRub have you covered in this colossal @ACSChemRev: bit.ly/3nHK0U4 Great pandemic collab w/ our friends in the @bfshi lab!
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Slightly belated but all recordings/materials from last quarter's virtual @ScrippsGradPrgm 2021 Organometallics Grad Course are now updated and freely available. Experience it yourself, connection drops included!😎 Videos: bit.ly/3xnbEsg Website: bit.ly/3jibBJw
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The final version of our #AmericasFinestCity collaboration @SDSU @UCSDChemBiochem @scrippsresearch is now #JustAccepted @angew_chem. Check out what Cu(CAAC) catalysts can do in alkyne protoborations and -silylations. bit.ly/3zOx2cp
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A new mechanistic take on alkene 1,2-carbosulfenylation that proceeds w/ syn-stereoselectivity. Check out the final version of #TeamNickel's study in @J_A_C_S this week, led by @ZiqiLi0513. bit.ly/3rx3j5t
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The final version of our free-amine-directed Ni-catalyzed alkene carboamination paper is now online @ACSCatalysis. Great stuff by @TaehoKang6 @jmanu3 @ZiqiLi0513 & #BMSChemistry! bit.ly/3w36t3W
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1st of a 2-part story (part 2 slated for next week!) showing how the hemilabile and redox-active properties of quinone ligands unlock 🔑 unprecedented scope in Ni-cat alkene additions: tinyurl.com/yc8dzj3c @chemrxiv @ZiqiLi0513 @0iTurki @ChicagOChemO @pengliu_group
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A new take on cyclopropanation by @NiHuiqi. An unusual collaboration that brings together chemists working on catalysis, high-energy materials (@Davin_lab), and medicines (#PfizerChemistry). @ChemRxiv pre-print: bit.ly/3LMfoyv
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I like my C-H bonds broken, not stirred.
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Humbled and honored to take the baton from Dean Phil @Dawson_Group and build on his remarkable tenure and legacy in this role.
Prof. Keary Engle of the @EngleLab is the new Dean of Graduate and Postdoctoral Studies at Scripps Research, leading the @ScrippsGradPrgm. An alumnus, Engle brings personal experience and is committed to mentoring future researchers. More: ow.ly/FcHR50Su8l2
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Start off your morning w/ a shot of alcohol. OH-directed alkene carboamination enabled by tailored N-electrophiles from @TaehoKang6 @Nana_Kem22 & #BMSChemistry in @ChemRxiv bit.ly/30Q1CSI. Cheers! 🍻 #itsfiveoclocksomewhere
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Starting Mon (Aug 3), OM Bootcamp @scrippsresearch is going virtual! This year we are opening it up to undergrads (esp those at PUIs!) who may have missed out on summer research. DM for details if you’d like to take part.
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An academic, a process chemist, and a catalyst manufacturer walk into a pre-print... tinyurl.com/4d8xfmy2 Take the plunge w/ us into the non-PGM catalyst pool!
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It's taken a few years of tinkering, but #TeamNickel & @pengliu_group are pleased to report the next chapter in regiodivergent alkene functionalization today in @ChemRxiv. New Pyrox ligand overcomes innate reactivity prefs. @ZiqiLi0513 @bamtran24 @gytyw bit.ly/3fwXQ6F
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#TeamNickel is already at it again in 2021! Together w/ #BMSChemistry colleagues, Nana, Van, and Omar describe Ni(COD)(DMFU), an all-in-one diarylation precatalyst bit.ly/3pUIe1J - part of the upcoming #Synlett @thiemechemistry Ni catalysis cluster.
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2021 OM Bootcamp @scrippsresearch kicks off next week Mon (Aug 9) in virtual/hybrid format, open to all. We are hoping to beat last year's undergrad turnout (esp those at PUIs)! Register here: forms.gle/Q8v9xnvpd6u4B5z28
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Teaching nitroalkanes to play nice with unactivated alkenes: bit.ly/3gbXV1r @ChemRxiv @ASimlandy
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In our lab's newest @ChemRxiv pre-print @sunjuntao1 & team craft C–N chiral axes through atroposelective C(heteroaryl)-H activation. Unique products that react fast & selectively in [4+2]s. tinyurl.com/47av296n
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Our collaboration on selective C(alkenyl)–H activation mediated by a transient directing group, together w/ @pengliu_group, is online in final form @angew_chem: bit.ly/38ik2CH Great team effort by @MYNoblemetal @sunjuntao1 @tugcegerbay @NiHuiqi @TitoBraulio!
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Pleased to share the final version of our 3-component alkenyl alcohol carboamination paper, now in @J_A_C_S by @TaehoKang6 @Nana_Kem22 #BMSChemistry: bit.ly/3gwnhYy
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Synthesize Pd(COD)(DQ) together with the master (Wenji @HarryHe88239850) and the apprentice (Keary). DM your shipping info for a free sample of the catalyst made by Keary himself. Thanks to @avrlisboa for awesome filming and editing! piped.video/watch?v=8UqbNgAm…
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What can we say? We 🧡🖤🧡 making heterocycles. (Carbocycles aren't bad either.) Happy to share the latest results from our collaboration w/ @pfizer led by @NiHuiqi on the Pd(II)/Pd(IV) anti-annulation of alkenes. @ChemRxiv bit.ly/3Cdhy2F
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Sequence-encoded monomers, a platform for translating difunctionalization into linear polymer backbones. A fun collaboration w/ @GuteGroup @pengliu_group & #BMSChemistry, appearing today in @NatureSynthesis. tinyurl.com/mujhve56
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A full account of our work on Ni(0)-cat directed Markovnikov hydroarylation and -alkenylation with RB(OH)2 is online today @ChemRxiv: 3 new protocols, >70 examples, and detailed mechanistic studies by #TeamNickel @ZiqiLi0513 @omar__apolinar and Ruohan. bit.ly/3yDc7c0
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After years of failures, frustration, and false starts... We are excited to share: chiral transient directing groups in Pd-cat alkene functionalization. Brilliant stuff by Luke and team @bamtran24 @tugcegerbay @pengliu_group. The force is strong w/ this one! #RealTimeChem
A Transient Directing Group Strategy Enables Enantioselective Reductive Heck Hydroarylation of Alkenes by Keary Engle (@EngleLab) & co-workers bit.ly/2kGI69O
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Move over @Padres, SD's got 🔥new team on the block @SDSU @UCSDChemBiochem @scrippsresearch. CAAC ligands 💪 in Cu-boryl alkyne additions (bit.ly/3g9n5z0) @ChemRxiv. Game day roster ⚾️: @gytyw @YazdaniSimaChem @JunorGlen @Rodolphe_Jazzar Grotjahn & Bertrand labs.
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Breaking bonds, taking names 😎Congrats to Van, John, and Kin on their Nat. Chem. paper describing a beta-X elimination approach to covalent bond activation. nature.com/articles/s41557-0…
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Now out in Acc Chem Res, @CamZRub @HarryHe88239850, & @stevewiz06 chart our journey together w/ #BMSChemistry towards practical Ni(0) catalysts. tinyurl.com/37u72u6x
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New additions to the synthetic 🧰 enabled by co-catalytic transient directing groups (TDGs). Enantioselective hydroalkenylation / hydroalkynylation & non-aromatic alkenyl aldehydes. Led by @ASimlandy. @ChemRxiv preprint: bit.ly/39gQUwr
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We are thankful for EDD ligands 🙏🏻 Coming soon…
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Still partying w/ Barry two weeks later @scrippsresearch @NobelPrize #clickchemistry 🎉🎈🎊
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Hey @ardemp this parking spot is open. @NobelPrize @scrippsresearch
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Ni-quinone 📖 Part 2 is online @J_A_C_S. @Yeongyu_Hwang designed a quinone ligand to enable 1,2-carboamidation via nitrenoid transfer. Using DFT, he traced the origin of enhanced reactivity to hemilability & ⏫ electrophilicity during migratory insertion. tinyurl.com/yus89484
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Highlight #3 from our non-PGM review (tinyurl.com/y52v356b) features @UyedaLab's Co-catalyzed cyclpropanation, deployed in the synthesis of nirmatrelvir by the #PfizerChemistry + Curia teams. A non-PGM catalysis triumph! tinyurl.com/443bvrve
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By popular demand, we are happy to offer video recordings of all lectures for Organometallics 2019 @scrippsresearch @ScrippsGradPrgm via @YouTube. Tune in, and let us know how we can make your remote learning experience as valuable as possible. englelab.com/resources/
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#4 After a technical delay at the end of 2023, we're finally ready to finish the countdown and share our lab's recent Ni review. The penultimate discovery to highlight comes from Knochel, who observed accelerated C(sp3)-C(sp3) coupling w/ an embedded EDO. tinyurl.com/fmmnepkh
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In the lab's latest review, @TaehoKang6 & @omar__apolinar dive into the state of play in asymmetric Ni- and Pd-catalyzed olefin dicarbofunctionalization. Thanks to the team at Synthesis @thiemechemistry for the invitation! thieme-connect.com/products/…
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Sometimes dreams (and dream rxns) come true! One of our dreams since 2015 has been to use simple carboxylates to direct alkene difunctionalization. @JD_Chimico, Taeho, and #TeamNickel brought the dream to life. Another fun collaboration with @stevewiz06 and #BMSChemistry.
Nickel-Catalyzed 1,2-Diarylation of Alkenyl Carboxylates: A Gateway to 1,2,3-Trifunctionalized Building Blocks by Keary Engle (@EngleLab) & co-workers bit.ly/2nReGHf
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Free the amines! bit.ly/3IE6lMg No PG, no problem for #TeamNickel in their most recent @ChemRxiv pre-print. Leaving group tuning 🔧 of the amine electrophile is the 🔑! @TaehoKang6 @jmanu3 @ZiqiLi0513 #BMSChemistry
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Fluorine meets its match 💪 in a sterically tuned directing auxiliary that can squeeze out pesky C(sp3)-F bonds from the metal center. A fun new @ChemRxiv pre-print brought to you by @liu_zhonglin #BMSChemistry & team: bit.ly/36L74wO
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Excited to offer samples of a new nickel(0) precatalyst from our collaboration with #BMSChemistry as part of today’s talk @StanfordUChem. Stop by at 4:30 pm to learn more. Air/water-stable ✅ Luggage-stable ✅ Pub coming soon! #TeamNickel @BurnsChemistry @du_bois_lab @YanXiaLab
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Our latest installment in alkene carbosulfenylation now tolerates alkylzinc nucleophiles, allowing for simultaneous C(sp3)-C(sp3) and C(sp3)-S bond formation @ChemicalScience @ZiqiLi0513: rsc.li/3vFjKPI
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Very grateful to @Amgen and excited share this recognition with the other 2020 awardees @veeslerlab @AlisonNarayanUM @jphilippejulien and Sergey Pronin.
“We are always searching for more efficient ways to discover compounds that improve human health.” Congratulations to organic #chemistry Prof. Keary Engle, who has received the Young Investigator Award from @Amgen scripps.edu/news-and-events/… @EngleLab #drugdiscovery
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Last year we celebrated Keary’s birthday 🎉 with the release of three chemrxiv preprints over three days 😎! This year we’re celebrating a month late due to the arrival of the newest and smolest Engle- baby Ollie 👶!
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5⃣-membered azaheterocycles as directing groups for olefin diarylation. #teamnickel strikes again! @yilincao_chem @ZiqiLi0513 Celebrating @morandilab's 2023 TYIA @ELSchemistry. Congrats Bill & team! tinyurl.com/2rs42zyw
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We congratulate our super 🌟🤩🌟 postdoc @SkylerMendoza2 for being awarded an @NSF #MPSAscend Postdoc Fellowship @scrippsresearch. Skyler is a @CaltechCCE @sarah_reisman lab alum who is applying his synthetic chops in organometallic catalysis. Bravo!
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#1 As we count down⌛️ to publication of our forthcoming nickel(0) review, we highlight milestones from other labs that paved 🛣️ the way. First up: the original synthesis of Ni(CO)4 (caution: volatile and toxic). tinyurl.com/mryfsr6n
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A classical rxn with a lot left to teach us. Check out the #JustAccepted version of our mechanistic deep dive into catalytic E/Z isomerization of alkenes w/ Pd(II) led by @MatsuuraRei together w/ @DonnaBlackmond in @ACSCatalysis, formerly @ChemRxiv. bit.ly/2PlzZhO
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CAAC ligand not afraid to put boron and carbon in their place. The latest installment of our all-SD tri-institutional collaboration on (CAAC)Cu catalysis appears today: bit.ly/3og1Ui0 @ChemRxiv @SDSU @UCSDChemBiochem @scrippsresearch
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Best of luck in the adventure ahead, Amit! We miss you already @scrippsresearch.
Thrilled to start my independent career as Assistant Professor in the department of Chemical sciences at @IISER_BERHAMPUR. Really grateful to @LabMukherjee @KBrownLab @EngleLab for the training and tremendous support during this journey.
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Engle lab students were rolling deep at #ACSSpring2022. @ZiqiLi0513 presented not 1 but 3 posters @NiHuiqi represented #teampalladium while Yilin and Taeho showed off their work with #teamnickel. Alena presented a talk as part of the cross coupling symposium. Great work everyone!
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#Thanksgiving appetizer served by #TeamNickel and #BMSChemistry 🍽🍗😋 — @omar__apolinar & team report on the unique ability of sulfonamides to direct challenging alkene 1,2-diarylation #JustAccepted @ACSCatalysis: bit.ly/3lQ2K1R
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Simple conditions ➡️ Strange selectivity. Alena and John’s work on α-selective hydroarylation of Michael acceptors with #BMSChemistry is #JustAccepted @J_A_C_S. Way to go team! bit.ly/2YO9F2P
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The final version of our @ASimlandy's olefin/nitroalkane coupling paper is now online @ACSCatalysis. Strikingly simple combination of PdI2, HFIP, and Na2CO3 enables this previously elusive addition w/ mechanistic details from @0iTurki @pengliu_group: bit.ly/3SIMCP1
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#2 Seminal WW2-era contribution from Kharasch @UChiChemistry documenting C(sp2)-C(sp2) cross-coupling catalyzed by nickel. 🤩 tinyurl.com/bdezauvk
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*Ringing* in 2022 🍾🔔🎉 w/ the final version of collaborative alkene annulation paper w/ our neighbors @pfizer, now online in @angew_chem: bit.ly/3G9hAKR. Well done @NiHuiqi & team!
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Kicking the week off w/ an alkene ➡️ heterocycle bonanza in @ChemRxiv bit.ly/3hPNXCz. A Larock-inspired alkene (hetero)annulation w/ @pfizer and @pengliu_group.
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🎂🍰🎊🎉 The Engle lab turns 3 today! Thanks to all coworkers for a great year of chemistry, and here’s to many more to come! @scrippsresearch
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Translating catalytic three-component difunctionalizations from alkenes to alkynes has proven harder than it looks. Now together w/ the @bfshi and Lan labs, @MYNoblemetal & @sunjuntao1 blaze a path to tetrasubstituted olefins via oxyhalogenation. @ChemRxiv bit.ly/3nwdwg5
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#3 From the MPI-Kofo, the heart of the organonickel revolution, comes Wilke's 1960 synthesis of Ni(COD)2 and Ni(CDT). At <500 words, every sentence packs a punch. tinyurl.com/y3j2p22e tinyurl.com/4hm69uk3
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Sulfonamides to the rescue! In a pre-print @ChemRxiv #TeamNickel describes how sulfonylation can enhance directing ability & enable N-functionalization of alkenyl amines. @omar__apolinar @bamtran24 @JD_Chimico #BMSChemistry bit.ly/2WgBpuL
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The people have spoken 🗳️!Our lab’s pick for paper of the month 🏆, as presented by Wenzhuo, is the collab study on enantioselective Ni-cat couplings of unactivated alkenes from the Koh & Shi labs @NatureCatalysis. @MJKoh87 nature.com/articles/s41929-0…
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Very honored to be included in this super talented cohort of 2019 #SloanFellows. Grateful to work with an awesome group of students, postdocs, and colleagues @scrippsresearch - a great team makes great research possible!
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Keepin’ 😎 while making 🟩s. In our latest pre-print w/ @pengliu_group and @pfizer we show how pi-stacking and other non-covalent interactions enable Cu-cat hydroboration of BCBs bit.ly/3gReTkn. Props to ⭐️ project leads @TaehoKang6 and @tugcegerbay!
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Very happy😀 to share the final versions of 2 papers today, both a long time in the making. The 1st from @liu_zhonglin & team w/ #BMSChemistry describes a selective 1,2-carbofluorination of unactivated alkenes under Pd catalysis @angew_chem: bit.ly/3EDDJTE
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What’ve you got against fumarates after that they’ve done for you @JD_Chimico?? @J_A_C_S pubs.acs.org/doi/10.1021/jac… #proudofalumni
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The final version of @ASimlandy's study is now online in @angew_chem: bit.ly/3paBy4d. New since the pre-print: @0iTurki's in-depth DFT study of the special feature of tert-leucine that make it such an effective TDG across different migrating groups (@pengliu_group).
New additions to the synthetic 🧰 enabled by co-catalytic transient directing groups (TDGs). Enantioselective hydroalkenylation / hydroalkynylation & non-aromatic alkenyl aldehydes. Led by @ASimlandy. @ChemRxiv preprint: bit.ly/39gQUwr
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Simple conditions, strange selectivity. Our newest alpha-selective hydroarylation work is online @ChemRxiv bit.ly/39ZDlN4. Nice method + mechanism story from Alena, John, and #BMSChemistry.
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The first paper from #TeamNickel in 2020 is in press at @angew_chem! Allyl electrophiles in conjunctive cross coupling with alkenes... What could possibly go wrong? Learn more: bit.ly/2GodJwp @bamtran24 @JD_Chimico @pengliu_group
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When Pd throws you a surprise party. @AndrewMRomine @ChemRxiv bit.ly/2MDxXIx
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For anyone who did not get a sample of Ni(COD)(DQ) earlier this year or needs another batch, it is now available from @MilliporeSigma bit.ly/3cmayDz
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Delighted to celebrate our amazing grads👨‍🎓@AndrewMRomine & @W0TangClan @ScrippsGradPrgm.
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“The science belongs to you, not to me.” -Coach Hans Renata @hanzyduzit Stunning science by our treasured friend and colleague during his promotion talk @scrippsresearch. 🥅⚽️💨🏃
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