BAE_Lab

@Bae_Lab

Group of Prof. Hanyong Bae @ Dept. Chemistry, SKKU. Reaction Design & Catalysis Lab.

Suwon, KOREA

Joined February 2018

387Following

250Followers

Pinned

BAE_Lab@Bae_Lab · Jan 29, 2024

Check out our new paper in Cell Reports Physical Science, entitled "Pinacolborane-assisted superacid organocatalysis enabled direct access to cytotoxic alkyl N-Cbz amines". Congratulations to Woo Hee! cell.com/cell-reports-p…

Bae_Lab's tweet card. Kim et al. demonstrate the direct synthesis of N-benzyloxycarbonyl alkyl amines using a superacid organocatalyst. Selective reductive amination provides access to a range of scaffolds, including...

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BAE_Lab@Bae_Lab · Jul 8

Thrilled to share our collaborative work with Prof. Yoonsu Park’s group published in Nature Communications: Superacid counteranion as flexible-coordinating ligand for asymmetric organo-bismuth catalysis. Congratulations to Jin Hyun and Seok Yeol! doi.org/10.1038/s41467…

Bae_Lab's tweet card. Nature Communications - Asymmetric binary catalysis combining chiral Brønsted acids with Lewis acids is currently limited to pre-organized, activated substrates. Here, the authors report...

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BAE_Lab@Bae_Lab · Jun 17

We are truly honored to have our recent contributions to "water-enhanced catalysis" featured in Accounts of Chemical Research, where we highlight its promise in expanding the landscape of modern catalysis pubs.acs.org/doi/10.1021/ac…

Bae_Lab's tweet card. ConspectusWater, an environmentally friendly and benign reaction medium, has traditionally been underestimated for its use in organic synthesis because it offers limited substrate solubility and can...

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BAE_Lab@Bae_Lab · Nov 13

A new paper collaboration with Prof. Min Sang Kwon's group (SNU) in Cell Reports Physical Science, "Water-accelerated single-electron transfer aquaphotocatalysis for open-chain SuFEx hubs" is now published. Congratulations to Byeongjun and Yonghwan! cell.com/cell-reports-p…

Bae_Lab's tweet card. Koo and Kwon et al. report a water-accelerated single-electron transfer aquaphotocatalytic approach to access alkyl SuFEx hubs. A variety of amines and carboxylic acids are efficiently converted into...

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BAE_Lab@Bae_Lab · Aug 23

A new paper entitled "Highly Functionalized SuFEx-able Hub Bearing All-Carbon Quaternary Center via Rapid Brønsted Superbase Catalysis" from our group is now available in Organic Letters. Congratulations Soyeon!! pubs.acs.org/doi/abs/10.102…

Bae_Lab's tweet card. A rapid Brønsted superbase catalysis for highly functionalized sulfur(VI)–fluoride exchange (SuFEx) hubs bearing all-carbon quaternary centers was developed. Remarkable functional group tolerance...

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BAE_Lab@Bae_Lab · May 8, 2024

Our new paper entitled "“On-Water” Accelerated Dearomative Cycloaddition via Aquaphotocatalysis" is now published in Nature Communications. Congratulations to Soo Bok! nature.com/articles/s4146…

Bae_Lab's tweet card. Nature Communications - Developing water compatible synthetic methods for Sulfur(VI) fluoride exchange (SuFEx) chemistry is of paramount importance. Here the authors demonstrate a catalytic...

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BAE_Lab@Bae_Lab · Jan 5, 2024

Glad to share our first publication this year @ChemCatalysis, trityl tetrakis(pentafluorophenyl)borate as a sustainable precursor in silylium Lewis acid organocatalysis! sciencedirect.com/science/articl…

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Jiwoong Lee@TheLeeLab_Chem · Oct 5, 2023

I finally visited my alma mater SKKU met old friends, mentors, and teachers after a long break. Thanks to @Bae_Lab for organizing the trip. Korea is certainly one of the most dynamic and vibrant countries which can contribute to the whole world in terms of R&D.

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Green Chemistry@green_rsc · Feb 20, 2023

Out in Green Chemistry 📢 A new PPM-level organocatalyst for metal-free, solvent-free, and purification-free cyanosilylation of ketones! A work from @Bae_Lab 🎉 Read here 👇 doi.org/10.1039/D3GC00…

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BAE_Lab@Bae_Lab · Feb 17, 2023

Our new paper entitled "Sustainable Oragnocatalytic Cyanosilylation of Ketones by PPM-Level Loading Triphenylcarbenium Tetrakis(pentafluorophenyl)borate" is now published in Green Chemistry. Congratulations Muhammad! pubs.rsc.org/en/content/art…

Bae_Lab's tweet card. Along with the significant demand for sustainable homogeneous catalysis, the importance of efficient synthesis and simple purification of complex organic compounds is attracting attention. Herein, we...

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BAE_Lab@Bae_Lab · Feb 10, 2023

A new paper "Alkyl Sulfonyl Fluorides Incorporating Geminal Dithioesters as SuFEx Click Hubs via Water-Accelerated Organosuperbase Catalysis", a collaborative work with Prof. Paul Ha-Yeon Cheong group is published in Org. Lett. Congratulations to all! pubs.acs.org/doi/full/10.10…

Bae_Lab's tweet card. Sulfur(VI) fluoride exchange (SuFEx) is recognized as another emerging tool for click chemistry. The preparation of the functionalized alkyl sulfonyl fluorides as key SuFEx hubs via C(sp3)–C(sp3)...

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BAE_Lab@Bae_Lab · Nov 10, 2022

Prof. Tsuji from Hokkaido University visited Bae Lab!!

NNobuyaTsuji@NobuyaTsuji · Nov 10, 2022

Annyeong from Korea!

BAE_Lab@Bae_Lab · Aug 27, 2022

We are happy to announce that Han Yong is selected as this year's recipient of the Young Organic Chemist Award at KCS Organic Chemistry Division, together with Prof. Jun-Seok Lee @junseoklee! Congratulations a lot to Prof. Bae and Prof. Lee!

Bae_Lab's tweet image. We are happy to announce that Han Yong is selected as this year's recipient of the Young Organic Chemist Award at KCS Organic Chemistry Division, together with Prof. Jun-Seok Lee @junseoklee! Congratulations a lot to Prof. Bae and Prof. Lee!

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AK List@ListLaboratory · Aug 12, 2022

We at #NobelPrize symposium to honor Ben. It was great to welcome our alumni back in Mülheim @maxplanckpress

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AK List@ListLaboratory · Aug 11, 2022

A bubbly welcome 🎉 #benlist2021 #nobelsymposium @NobelPrize @maxplanckpress

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Ashwani_Kumar ⬅️ Ph.D.@Ashwani_Kumar_2 · Aug 11, 2022

Wow...a night to remember, 💥💥 most awaited event of #MPIKOFO .. celebrating Nobel prize 2021 of Nobel laureate Prof. List. @ListLaboratory @JinsunLee11 @Bae_Lab #Nobel_Prize

BAE_Lab@Bae_Lab · Jul 8, 2022

Our group published a new paper in ChemSusChem, entitled "β-Aminosulfonyl Fluorides via Water-Accelerated N-Heterocyclic Carbene Catalysis". Congratulations to Jin Hyun!! …mistry-europe.onlinelibrary.wiley.com/doi/10.1002/cs…

Bae_Lab's tweet card. Just add water: A new remarkable water-accelerated noncovalent N-heterocyclic carbene catalysis of an aza-Michael addition reaction enables access to β-aminosulfonyl fluorides, which is key hub for...

BAE_Lab@Bae_Lab · May 31, 2022

Today, we published a new paper in ChemSusChem, entitled "Hydrophobic Amplification Enabled High-Turnover Phosphazene Superbase Catalysis". Many congratulations to Sun Bu!! …mistry-europe.onlinelibrary.wiley.com/doi/10.1002/cs…

Bae_Lab's tweet card. Superbase: β-Sulfido sulfonyl fluorides are attractive structures as potentially useful inhibitors and organic materials. Here a significant “on-water” hydrophobic amplification enables a high-turn...

BAE_Lab@Bae_Lab · May 17, 2022

Our group published a paper entitled "Efficient Access to General α-Tertiary Amines via Water-Accelerated Organocatalytic Multicomponent Allylation" in Nature Communications! Many congratulations on all members involved!! nature.com/articles/s4146…

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AK List@ListLaboratory · May 4, 2022

Breakthrough for organocatalysis: a highly challenging reaction of a small unbiased substrate toward a pharmaceutically relevant product is accomplished with better than enzymatic selectivity. Our recent work @Nature by @huizhou91983288 nature.com/articles/s4158…

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