Year |
Citation |
Score |
2022 |
Zhang Z, Bera S, Fan C, Hu X. Streamlined Alkylation via Nickel-Hydride-Catalyzed Hydrocarbonation of Alkenes. Journal of the American Chemical Society. PMID 35413202 DOI: 10.1021/jacs.1c13482 |
0.533 |
|
2021 |
Mao R, Bera S, Turla AC, Hu X. Addition to "Copper-Catalyzed Intermolecular Functionalization of Unactivated C(sp)-H Bonds and Aliphatic Carboxylic Acids". Journal of the American Chemical Society. 143: 17302. PMID 34632758 DOI: 10.1021/jacs.1c10082 |
0.714 |
|
2021 |
Mao R, Bera S, Turla AC, Hu X. Copper-Catalyzed Intermolecular Functionalization of Unactivated C(sp)-H Bonds and Aliphatic Carboxylic Acids. Journal of the American Chemical Society. PMID 34463489 DOI: 10.1021/jacs.1c05874 |
0.708 |
|
2021 |
Bera S, Mao R, Hu X. Publisher Correction: Enantioselective C(sp)-C(sp) cross-coupling of non-activated alkyl electrophiles via nickel hydride catalysis. Nature Chemistry. PMID 33558738 DOI: 10.1038/s41557-021-00649-7 |
0.698 |
|
2021 |
Qian D, Bera S, Hu X. Chiral Alkyl Amine Synthesis via Catalytic Enantioselective Hydroalkylation of Enecarbamates. Journal of the American Chemical Society. PMID 33481564 DOI: 10.1021/jacs.0c11630 |
0.575 |
|
2020 |
Bera S, Mao R, Hu X. Enantioselective C(sp)-C(sp) cross-coupling of non-activated alkyl electrophiles via nickel hydride catalysis. Nature Chemistry. PMID 33380741 DOI: 10.1038/s41557-020-00576-z |
0.724 |
|
2019 |
Mao R, Bera S, Cheseaux A, Hu X. Deoxygenative trifluoromethylthiolation of carboxylic acids. Chemical Science. 10: 9555-9559. PMID 32055327 DOI: 10.1039/C9Sc03396C |
0.684 |
|
2019 |
Bera S, Hu X. Nickel-Catalyzed Regioselective Hydroalkylation and Hydroarylation of Alkenyl Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 31282601 DOI: 10.1002/Anie.201907045 |
0.623 |
|
2017 |
Bera S, Daniliuc CG, Studer A. Oxidative N-Heterocyclic Carbene Catalyzed Dearomatization of Indoles to Spirocyclic Indolenines with a Quaternary Carbon Stereocenter. Angewandte Chemie (International Ed. in English). PMID 28471010 DOI: 10.1002/Anie.201701485 |
0.586 |
|
2017 |
List B, Gatzenmeier T, Bera S, Daniliuc CG, Studer A. N-Heterocyclic Carbene Catalyzed Oxidative Spirocyclization of Indoles Synfacts. 13: 875-7406. DOI: 10.1055/S-0036-1590690 |
0.459 |
|
2017 |
Bera S, Daniliuc CG, Studer A. Cover Picture: Oxidative N‐Heterocyclic Carbene Catalyzed Dearomatization of Indoles to Spirocyclic Indolenines with a Quaternary Carbon Stereocenter (Angew. Chem. Int. Ed. 26/2017) Angewandte Chemie. 56: 7321-7321. DOI: 10.1002/Anie.201704766 |
0.507 |
|
2017 |
Bera S, Daniliuc CG, Studer A. Titelbild: Durch N-heterocyclische Carbene katalysierte oxidative Dearomatisierung von Indolen zu spirocyclischen Indoleninen mit quartärem Stereozentrum (Angew. Chem. 26/2017) Angewandte Chemie. 129: 7427-7427. DOI: 10.1002/Ange.201704766 |
0.46 |
|
2017 |
Bera S, Daniliuc CG, Studer A. Durch N‐heterocyclische Carbene katalysierte oxidative Dearomatisierung von Indolen zu spirocyclischen Indoleninen mit quartärem Stereozentrum Angewandte Chemie. 129: 7508-7512. DOI: 10.1002/Ange.201701485 |
0.465 |
|
2016 |
Cramer D, Bera S, Studer A. Exploring Cooperative Effects in Oxidative NHC Catalysis - Regioselective Acylation of Carbohydrates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27038068 DOI: 10.1002/Chem.201601398 |
0.571 |
|
2016 |
Bera S, Studer A. Preparation of 4,6-Disubstituted α-Pyrones by Oxidative N-Heterocyclic Carbene Catalysis Synthesis. 49: 121-126. DOI: 10.1055/S-0036-1588336 |
0.552 |
|
2015 |
Bera S, Daniliuc CG, Studer A. Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis. Organic Letters. 17: 4940-3. PMID 26447330 DOI: 10.1021/Acs.Orglett.5B01932 |
0.606 |
|
2014 |
Bera S, Samanta RC, Daniliuc CG, Studer A. Asymmetric synthesis of highly substituted β-lactones through oxidative carbene catalysis with LiCl as cooperative Lewis acid. Angewandte Chemie (International Ed. in English). 53: 9622-6. PMID 25044490 DOI: 10.1002/Anie.201405200 |
0.517 |
|
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