Dr. Reg So

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Dr. Reg So

Dr. Reg So

@reg_so

organic chemistry, photo-triggered processes, DNA-templated synthesis

New York, NY Katılım Nisan 2012
2.7K Takip Edilen719 Takipçiler
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Dr. Reg So
Dr. Reg So@reg_so·
Happy to share that our seminal work on waixenicin A derivatization is now covered by a provisional patent: “Waixenicin A Derivatives as Neuroprotective Agents against Hypoxic Ischemic Brain Injury Through TRPM7 Blockade.” @RomoGrp_Baylor
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Science Magazine
Science Magazine@ScienceMagazine·
Researchers in Science report a kilogram-scale synthesis of enlicitide, a peptide drug for lowering low-density cholesterol that is in a Phase 3 clinical trial. This new synthesis route leverages engineered enzymes and crystallization of key intermediates, substantially cutting down the number of reaction steps while improving yield. Learn more in a new #SciencePerspective: scim.ag/4wmd0n5
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KoenigChemistry
KoenigChemistry@ChemistryKoenig·
A mild strategy compatible with various solvents, air, and moisture @angew_chem Congratulations to all involved! Geminal Difunctionalization of Ketones via C─S Bond Insertion of Photogenerated Donor–Donor Diazo Compounds doi.org/10.1002/anie.6…
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Yulab
Yulab@YulabJin·
Methylene CH can now be coupled with Aryl CH. The scope is limited, but what new ligand can do is always a pleasant surprise: pubs.acs.org/articlesonrequ…
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Yang Yang
Yang Yang@yang2biocat·
In @NatureCatalysis we report the integration of photoredox radical generation and metal-carbenoid chemistry to achieve a formal metal carbenoid-radical coupling with enzymatic stereocontrol: nature.com/articles/s4192…
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Ritter Lab
Ritter Lab@ritter_lab·
In @Nature, we show that redox-active esters can be transformed into alkyl zinc species useful for transmetalation, providing a solution to rate matching in XEC reactions! First application: alkylation of alkenes via polar decarboxylative cross-coupling! nature.com/articles/s4158…
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Andy McNally
Andy McNally@AndyMcNally367·
A new direction in our pyridine phosphonium ion program: Phosphonium Ions as Activating Groups for the Selective Alkylation of Pyridines and Polyazines. chemrxiv.org/doi/full/10.26…
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Milner Group at Cornell University
Check out team MOFganic's newest entry, out now in @J_A_C_S! Superstar PhD student Yihuan showed that MOFs allow for dosage delivery of simple fluorinated gases, enabling switchable control over borylated vs iodinated product formation in electroreductive radical reactions.
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Science Magazine
Science Magazine@ScienceMagazine·
For decades, biology textbooks have enshrined a simple rule: DNA is made by copying a template. After one enzyme unzips a DNA double helix into separate strands, another called a polymerase builds a complementary sequence, base by base, for each strand. Presto: two copies of the original DNA. But new research into how bacteria defend themselves from viruses now shows this synthesis rule isn’t absolute. Now, a team describes a bacterial enzyme that synthesizes DNA without a nucleic acid template, using its own structure as a guide. Learn more: scim.ag/4tTc5IA @NewsfromScience
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Yamaguchi Lab
Yamaguchi Lab@jyamaguchilab·
Our review article is now out in Chemical Communications: “Nitrogen Editing of Aromatic Rings: From Skeletal Editing to Fragment Editing.” Congratulations to Hikaru!! Two days in a row!! doi.org/10.1039/D6CC01…
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Yamaguchi Lab
Yamaguchi Lab@jyamaguchilab·
Our latest review has been published in Organic Chemistry Frontiers @OrgChemFront : “α-Borylcarbene Precursors: Design, Generation, and Synthetic Opportunities” doi.org/10.1039/D6QO00… Big congratulations to Ryuya and Kei @DJmuto !!
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Magnus Rueping
Magnus Rueping@Rueping_Lab·
We are pleased to share our Nat Rev Chem review! We summarize how photo-, electro-, and electrophotochemical strategies are reshaping C–N bond formation, distinguishing them from traditional metal catalysis toward more sustainable synthesis. @natrevchem dlvr.it/TS7DlQ
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