| Year |
Citation |
Score |
| 2022 |
Wang X, Li J, Hayashi Y. Highly Sterically Hindered Peptide Bond Formation between α,α-Disubstituted α-Amino Acids and -Alkyl Cysteines Using α,α-Disubstituted α-Amidonitrile. Journal of the American Chemical Society. 144: 10145-10150. PMID 35658430 DOI: 10.1021/jacs.2c02993 |
0.467 |
|
| 2021 |
Wang X, Li J, Hayashi Y. Oxidative peptide bond formation of glycine-amino acid using 2-(aminomethyl)malononitrile as a glycine unit. Chemical Communications (Cambridge, England). 57: 4283-4286. PMID 33913954 DOI: 10.1039/d1cc00130b |
0.422 |
|
| 2021 |
Li J, Lear MJ, Hayashi Y. Direct Cyclopropanation of α-Cyano β-Aryl Alkanes by Light Mediated Single Electron Transfer between Donor-Acceptor Pairs. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33565170 DOI: 10.1002/chem.202100341 |
0.463 |
|
| 2020 |
Bauer A, Di Mauro G, Li J, Maulide N. An α-Cyclopropanation of Carbonyl Derivatives by Oxidative Umpolung. Angewandte Chemie (International Ed. in English). PMID 32808419 DOI: 10.1002/Anie.202007439 |
0.517 |
|
| 2019 |
Li J, Oost R, Maryasin B, González L, Maulide N. A redox-neutral synthesis of ketones by coupling of alkenes and amides. Nature Communications. 10: 2327. PMID 31127092 DOI: 10.1038/S41467-019-10151-X |
0.526 |
|
| 2019 |
Li J, Bauer A, Di Mauro G, Maulide N. a-Arylation of Carbonyl Compounds by Oxidative C-C Bond Activation. Angewandte Chemie (International Ed. in English). PMID 31112360 DOI: 10.1002/Anie.201904899 |
0.522 |
|
| 2019 |
Li J, Preinfalk A, Maulide N. Diastereo- and Enantioselective Access to Stereotriads through a Flexible Coupling of Substituted Aldehydes and Alkenes. Angewandte Chemie (International Ed. in English). PMID 30919530 DOI: 10.1002/Anie.201900801 |
0.53 |
|
| 2019 |
Brutiu BR, Bubeneck WA, Cvetkovic O, Li J, Maulide N. On the formation of seven-membered rings by arene-ynamide cyclization. Monatshefte Fur Chemie. 150: 3-10. PMID 30662090 DOI: 10.1007/S00706-018-2320-X |
0.46 |
|
| 2019 |
Li J, Berger M, Zawodny W, Simaan M, Maulide N. A Chemoselective α-Oxytriflation Enables the Direct Asymmetric Arylation of Amides Chem. 5: 1883-1891. DOI: 10.1016/J.Chempr.2019.05.006 |
0.594 |
|
| 2019 |
Li J, Bauer A, Di Mauro G, Maulide N. α‐Arylierung von Carbonylverbindungen mittels oxidativer C‐C‐Bindungsaktivierung Angewandte Chemie. 131: 9921-9924. DOI: 10.1002/Ange.201904899 |
0.452 |
|
| 2019 |
Li J, Preinfalk A, Maulide N. Eine flexible Kupplung von Aldehyden und Alkenen ermöglicht die diastereo‐ und enantioselektive Herstellung von Stereotriaden Angewandte Chemie. 131: 5947-5950. DOI: 10.1002/Ange.201900801 |
0.46 |
|
| 2018 |
Li J, Preinfalk A, Maulide N. Enantioselective Redox-Neutral Coupling of Aldehydes and Alkenes by an Iron-Catalyzed "Catch-Release" Tethering Approach. Journal of the American Chemical Society. PMID 30576130 DOI: 10.1021/Jacs.8B12242 |
0.464 |
|
| 2018 |
Adler P, Pons A, Li J, Heider J, Brutiu BR, Maulide N. Chemoselective Activation of Diethyl Phosphonates: A Modular Synthesis of Biologically Relevant Phosphonylated Scaffolds. Angewandte Chemie (International Ed. in English). PMID 30067301 DOI: 10.1002/Anie.201806343 |
0.523 |
|
| 2018 |
Li J, Lear MJ, Hayashi Y. Autoinductive conversion of α,α-diiodonitroalkanes to amides and esters catalysed by iodine byproducts under O. Chemical Communications (Cambridge, England). PMID 29868676 DOI: 10.1039/C8Cc03191F |
0.467 |
|
| 2018 |
Adler P, Pons A, Li J, Heider J, Brutiu BR, Maulide N. Chemoselektive Aktivierung von Diethylphosphonaten: modulare Synthese von biologisch relevanten phosphonylierten Grundgerüsten Angewandte Chemie. 130: 13514-13518. DOI: 10.1002/Ange.201806343 |
0.502 |
|
| 2017 |
Baldassari LL, de la Torre A, Li J, Lüdtke DS, Maulide N. Ynamide Preactivation Allows a Regio- and Stereoselective Synthesis of α,β-disubstituted Enamides. Angewandte Chemie (International Ed. in English). PMID 29032598 DOI: 10.1002/Anie.201709128 |
0.696 |
|
| 2017 |
Baldassari LL, de la Torre A, Li J, Lüdtke DS, Maulide N. Regio- und stereoselektive Synthese α,β-disubstituierter Enamide durch Voraktivierung von Inamiden Angewandte Chemie. 129: 15929-15933. DOI: 10.1002/Ange.201709128 |
0.557 |
|
| 2016 |
Li J, Lear MJ, Hayashi Y. Sterically Demanding Oxidative Amidation of α-Substituted Malononitriles with Amines Using O2. Angewandte Chemie (International Ed. in English). PMID 27300467 DOI: 10.1002/Anie.201603399 |
0.501 |
|
| 2016 |
Li J, Lear MJ, Kwon E, Hayashi Y. Mechanism of Oxidative Amidation of Nitroalkanes with Oxygen and Amine Nucleophiles by Using Electrophilic Iodine. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26938791 DOI: 10.1002/Chem.201600540 |
0.487 |
|
| 2015 |
Li J, Lear MJ, Kawamoto Y, Umemiya S, Wong AR, Kwon E, Sato I, Hayashi Y. Oxidative Amidation of Nitroalkanes with Amine Nucleophiles using Molecular Oxygen and Iodine. Angewandte Chemie (International Ed. in English). PMID 26349836 DOI: 10.1002/Anie.201505192 |
0.454 |
|
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