![Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/cfd2d3c5-5966-498a-aa0d-befd86590017/ejoc202100526-toc-0001-m.jpg)
Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library
![Alkyne Aminopalladation/Heck and Suzuki Cascades: An Approach to Tetrasubstituted Enamines - Geffers - 2021 - Chemistry – A European Journal - Wiley Online Library Alkyne Aminopalladation/Heck and Suzuki Cascades: An Approach to Tetrasubstituted Enamines - Geffers - 2021 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/5d521f9d-e481-4632-bd56-c4343d54fbf8/chem202103567-toc-0001-m.jpg)
Alkyne Aminopalladation/Heck and Suzuki Cascades: An Approach to Tetrasubstituted Enamines - Geffers - 2021 - Chemistry – A European Journal - Wiley Online Library
![Isolation of an N‐Heterocyclic Carbene Complex of a Borasilene - Franz - 2019 - Chemistry – A European Journal - Wiley Online Library Isolation of an N‐Heterocyclic Carbene Complex of a Borasilene - Franz - 2019 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0cee98c0-e1ce-48dc-9da8-d5ed2d6d7a4d/chem201902877-toc-0001-m.png)
Isolation of an N‐Heterocyclic Carbene Complex of a Borasilene - Franz - 2019 - Chemistry – A European Journal - Wiley Online Library
![Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles | Chemical Reviews Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles | Chemical Reviews](https://pubs.acs.org/cms/10.1021/cr1004088/asset/images/medium/cr-2010-004088_0002.gif)
Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles | Chemical Reviews
![Preparation of Quaternary Centers via Nickel-Catalyzed Suzuki–Miyaura Cross-Coupling of Tertiary Sulfones | Journal of the American Chemical Society Preparation of Quaternary Centers via Nickel-Catalyzed Suzuki–Miyaura Cross-Coupling of Tertiary Sulfones | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.7b10855/asset/images/medium/ja-2017-10855f_0005.gif)
Preparation of Quaternary Centers via Nickel-Catalyzed Suzuki–Miyaura Cross-Coupling of Tertiary Sulfones | Journal of the American Chemical Society
Dual infection system identifies a crucial role for PKAâ•'mediated serine phosphorylation of the EPECâ•'Tirâ•'inj
![Molecular photoswitches in aqueous environments - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D0CS00547A Molecular photoswitches in aqueous environments - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D0CS00547A](https://pubs.rsc.org/image/article/2021/CS/d0cs00547a/d0cs00547a-f28.gif)
Molecular photoswitches in aqueous environments - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D0CS00547A
![Reaction of Azides with Dichloroindium Hydride: Very Mild Production of Amines and Pyrrolidin-2-imines through Possible Indium−Aminyl Radicals | Organic Letters Reaction of Azides with Dichloroindium Hydride: Very Mild Production of Amines and Pyrrolidin-2-imines through Possible Indium−Aminyl Radicals | Organic Letters](https://pubs.acs.org/cms/10.1021/ol0606637/asset/images/large/ol0606637n00001.jpeg)
Reaction of Azides with Dichloroindium Hydride: Very Mild Production of Amines and Pyrrolidin-2-imines through Possible Indium−Aminyl Radicals | Organic Letters
![Palladium‐Catalyzed Suzuki Coupling of N‐Acyloxazolidinones via Selective Cleavage of C–N Bonds - Jian - 2020 - European Journal of Organic Chemistry - Wiley Online Library Palladium‐Catalyzed Suzuki Coupling of N‐Acyloxazolidinones via Selective Cleavage of C–N Bonds - Jian - 2020 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/42bbf6d6-1da6-4842-8b96-38b9049b0c1d/ejoc202000575-toc-0001-m.jpg)
Palladium‐Catalyzed Suzuki Coupling of N‐Acyloxazolidinones via Selective Cleavage of C–N Bonds - Jian - 2020 - European Journal of Organic Chemistry - Wiley Online Library
![Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/c65dc490-f758-4875-ba85-b4baf9f9ba94/ejoc202100526-bio-0007-m.jpg)
Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library
![Synthesis of aryldifluoromethyl aryl ethers via nickel-catalyzed suzuki cross-coupling between aryloxydifluoromethyl bromides and boronic acids | Communications Chemistry Synthesis of aryldifluoromethyl aryl ethers via nickel-catalyzed suzuki cross-coupling between aryloxydifluoromethyl bromides and boronic acids | Communications Chemistry](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs42004-022-00694-4/MediaObjects/42004_2022_694_Fig1_HTML.png)
Synthesis of aryldifluoromethyl aryl ethers via nickel-catalyzed suzuki cross-coupling between aryloxydifluoromethyl bromides and boronic acids | Communications Chemistry
![Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/ce67a99c-1a78-4da5-b68f-621afe6be848/ejoc202100526-fig-5001-m.jpg)
Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues - Vries - 2021 - European Journal of Organic Chemistry - Wiley Online Library
![PDF) A simplified LC-MS/MS method for the quantification of the cardiovascular disease (CVD) biomarker trimethylamine-N-oxide (TMAO) and its precursors PDF) A simplified LC-MS/MS method for the quantification of the cardiovascular disease (CVD) biomarker trimethylamine-N-oxide (TMAO) and its precursors](https://i1.rgstatic.net/publication/350438273_A_simplified_LC-MSMS_method_for_the_quantification_of_the_cardiovascular_disease_CVD_biomarker_trimethylamine-N-oxide_TMAO_and_its_precursors/links/6140fb4cea4aa80011046f80/largepreview.png)