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Krische Lab Profile
Krische Lab

@KrischeLab

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Synthetic Methods and Natural Product Synthesis @ UT Austin

Austin, TX
Joined January 2019
Don't wanna be here? Send us removal request.
@KrischeLab
Krische Lab
9 days
The Austin-Gifu chemistry connection continues with a visit from Prof. Eiji Yamaguchi!
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@grok
Grok
25 days
Generate videos in just a few seconds. Try Grok Imagine, free for a limited time.
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@KrischeLab
Krische Lab
1 month
It's official! The third biennial WCSC is Nov. 15th, co-hosted by the @hull_group. Undergrads, grad students, post-docs, and faculty are welcome to register here: Thank you to our sponsors @Amgen @genentech @pfizer @AmerChemSociety. Hope to see you there!
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@KrischeLab
Krische Lab
2 months
Many thanks to former group members for their hospitality in Tokyo!
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@KrischeLab
Krische Lab
3 months
Many thanks to colleagues at Tohoku University for a wonderful visit!
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@KrischeLab
Krische Lab
4 months
Return of T-Schempp (aka Tabitha), destroyer of Soraphen and star alumnus at Eli Lilly, San Diego!
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@KrischeLab
Krische Lab
4 months
Congratulations to Prof. Yu-Rong Yang on the total synthesis of rubriflordilactone A via late-stage Ir-catalyzed 2-(alkoxycarbonyl)allylation!
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@KrischeLab
Krische Lab
4 months
From Texas to Tokyo - Great Colleagues, Great Chemistry!
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@KrischeLab
Krische Lab
6 months
This abundant, safe and environmentally benign hydrogen transfer agent enables this method to bypass the conversion of organic halides to premetalated cross-coupling partners using hazardous organometallic reagents (3/3). @NatureChemistry @genentech @PittTweet @UMNews.
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@KrischeLab
Krische Lab
6 months
In breakthrough work with researchers at Genentech, University of Pittsburgh and University of Minnesota, the Krische laboratory has merged these two processes, enabling direct cross-coupling of organic halides via hydrogen transfer using sodium formate (2/3).
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@KrischeLab
Krische Lab
6 months
Catalytic hydrogenation and metal-catalyzed cross-coupling are among the most broadly utilized methods in small-molecule drug discovery and manufacture (1/3).
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nature.com
Nature Chemistry - Transfer hydrogenation is challenging to apply to aryl halide reductive cross-couplings because of competing hydrogenolysis. Now aryl halide cross-couplings mediated by sodium...
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@KrischeLab
Krische Lab
7 months
A big thanks to Dylan Snelson and the students of SCRIPPS for a day filled with exciting science, including the honor of meeting one of my chemistry heroes, Prof. Barry Sharpless!
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@KrischeLab
Krische Lab
7 months
Congrats to Prof. Krische, who has been awarded the 2025 Yamada-Koga Prize for his breakthrough work on enantioselective C-C coupling via hydrogenation and transfer hydrogenation!.
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@KrischeLab
Krische Lab
8 months
Congratulations to “team ruthenium” on unlocking a broad, new (and directing-group-free) method for heteroaryl C-H functionalization using our concept of hydrogen auto-transfer! @J_A_C_S .
pubs.acs.org
A novel mechanism for N-heteroaryl C–H functionalization via dearomative addition-hydrogen autotransfer is described. Upon exposure to the catalyst derived from RuHCl(CO)(PPh3)3 and Xantphos, dienes...
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@KrischeLab
Krische Lab
9 months
Best Christmas gift ever from best students ever! They know me too well! Remember, vitamin D(og) is essential for good health!
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@KrischeLab
Krische Lab
9 months
Congratulations to Jessica and Kate on their Chemical Reviews article summarizing the many applications of our catalytic methods in natural product total synthesis. @ACSChemRev.
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pubs.acs.org
Catalytic enantioselective hydrogen autotransfer reactions for the direct conversion of lower alcohols to higher alcohols are catalogued and their application to the total synthesis of polyketide...
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@KrischeLab
Krische Lab
11 months
Congratulations to Guanyu (Brad) Hu, Rosalie Doerksen and Brett Ambler on completing the first total synthesis of type II polyketide antibiotic formicamycin H! @J_A_C_S .
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pubs.acs.org
The first total synthesis of the pentacyclic phenylnaphthacenoid type II polyketide antibiotic formicamycin H is described. A key feature of the synthesis involves the convergent, regioselective...
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@KrischeLab
Krische Lab
1 year
Congratulations to Cate, Sarah, Maddie and Jon on this fundamental contribution to catalytic cross-coupling beyond premetalated reagents or metallic reductants! @JOC_OL .
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pubs.acs.org
Formate-mediated reductive cross-couplings of vinyl halides with aryl iodides via palladium(I) catalysis occur with highly uncommon cine-substitution. The active dianionic palladium(I) catalyst,...
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