☰

Anat Milo, Ph.D. - Publications

Affiliations: 
2015- Chemistry Ben-Gurion University of the Negev, Be'er Sheva, South District, Israel 
Area:
physical organic chemistry
Website:
anatmilo.com
Tree Info Similar researchers PubMed Report error

17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Wang YZ, Wang ZH, Eshel IL, Sun B, Liu D, Gu YC, Milo A, Mei TS. Nickel/biimidazole-catalyzed electrochemical enantioselective reductive cross-coupling of aryl aziridines with aryl iodides. Nature Communications. 14: 2322. PMID 37087477 DOI: 10.1038/s41467-023-37965-0  0.624
2022 Alassad Z, Nandi A, Kozuch S, Milo A. Reactivity and Enantioselectivity in NHC Organocatalysis Provide Evidence for the Complex Role of Modifications at the Secondary Sphere. Journal of the American Chemical Society. PMID 36535039 DOI: 10.1021/jacs.2c08302  0.413
2022 Alassad Z, AboRaed A, Mizrachi MS, Pérez-Temprano MH, Milo A. Metal-Free Multicomponent Strategy for Amidine Synthesis. Journal of the American Chemical Society. 144: 20672-20679. PMID 36318611 DOI: 10.1021/jacs.2c07918  0.42
2022 Domb I, Lustosa DM, Milo A. Secondary-sphere modification in proline catalysis: old friend, new connection. Chemical Communications (Cambridge, England). 58: 1950-1953. PMID 35043796 DOI: 10.1039/d1cc05589e  0.488
2022 Lustosa DM, Barkai S, Domb I, Milo A. Effect of Solvents on Proline Modified at the Secondary Sphere: A Multivariate Exploration. The Journal of Organic Chemistry. 87: 1850-1857. PMID 35019660 DOI: 10.1021/acs.joc.1c02778  0.436
2020 Raed AA, Dhayalan V, Barkai S, Milo A. -Heterocyclic Carbene Triazolium Salts Containing Brominated Aromatic Motifs: Features and Synthetic Protocol. Chimia. 74: 878-882. PMID 33243323 DOI: 10.2533/chimia.2020.878  0.441
2019 Dhayalan V, Gadekar SC, Alassad Z, Milo A. Unravelling mechanistic features of organocatalysis with in situ modifications at the secondary sphere. Nature Chemistry. PMID 31086303 DOI: 10.1038/s41557-019-0258-1  0.479
2019 Dhayalan V, Mal K, Milo A. Practical Synthesis of Chiral N-Heterocyclic Carbene Triazolium Salts Containing a Hydroxy Functional Handle Synthesis. 51: 2845-2864. DOI: 10.1055/S-0037-1611786  0.38
2016 Santiago CB, Milo A, Sigman MS. Developing a Modern Approach to Account for Steric Effects in Hammett-type Correlations. Journal of the American Chemical Society. PMID 27652906 DOI: 10.1021/Jacs.6B08799  0.58
2016 Sigman MS, Harper KC, Bess EN, Milo A. The Development of Multidimensional Analysis Tools for Asymmetric Catalysis and Beyond. Accounts of Chemical Research. PMID 27220055 DOI: 10.1021/Acs.Accounts.6B00194  0.628
2016 Niemeyer ZL, Milo A, Hickey DP, Sigman MS. Parameterization of phosphine ligands reveals mechanistic pathways and predicts reaction outcomes. Nature Chemistry. 8: 610-7. PMID 27219707 DOI: 10.1038/Nchem.2501  0.574
2016 Neel AJ, Milo A, Sigman MS, Toste FD. Enantiodivergent Fluorination of Allylic Alcohols: Data Set Design Reveals Structural Interplay between Achiral Directing Group and Chiral Anion. Journal of the American Chemical Society. PMID 26967114 DOI: 10.1021/Jacs.6B00356  0.611
2015 Milo A, Neel AJ, Toste FD, Sigman MS. Organic chemistry. A data-intensive approach to mechanistic elucidation applied to chiral anion catalysis. Science (New York, N.Y.). 347: 737-43. PMID 25678656 DOI: 10.1126/Science.1261043  0.683
2014 Milo A, Bess EN, Sigman MS. Interrogating selectivity in catalysis using molecular vibrations. Nature. 507: 210-4. PMID 24622199 DOI: 10.1038/Nature13019  0.567
2012 Milo A, Neumann R. Achiral ruthenium catalyst encapsulated in titanium phosphonate homochiral peptide-based solids for enantioselective hydrogenation of ketones to secondary alcohols Acs Catalysis. 2: 2531-2536. DOI: 10.1021/Cs3005715  0.633
2011 Milo A, Neumann R. An achiral manganese salen catalyst encapsulated in a peptidic phosphonate homochiral solid for the enantioselective formation of diols by consecutive epoxidation and hydration reactions. Chemical Communications (Cambridge, England). 47: 2535-7. PMID 21225044 DOI: 10.1039/C0Cc04205F  0.629
2010 Milo A, Neumann R. A tripodal peptidic titanium phosphonate as a homochiral porous solid medium for the heterogeneous enantioselective hydration of epoxides Advanced Synthesis and Catalysis. 352: 2159-2165. DOI: 10.1002/Adsc.201000373  0.537
Show low-probability matches.