| Year |
Citation |
Score |
| 2023 |
Sinnema EG, Ramspoth TF, Bouma RH, Ge L, Harutyunyan SR. Enantioselective Hydrophosphination of Terminal Alkenyl Aza-Heteroarenes. Angewandte Chemie (International Ed. in English). e202316785. PMID 38133954 DOI: 10.1002/anie.202316785 |
0.377 |
|
| 2023 |
Postolache R, Pérez JM, Castiñeira Reis M, Ge L, Sinnema EG, Harutyunyan SR. Manganese(I)-Catalyzed Asymmetric Hydrophosphination of α,β-Unsaturated Carbonyl Derivatives. Organic Letters. 25: 1611-1615. PMID 36892214 DOI: 10.1021/acs.orglett.2c04256 |
0.368 |
|
| 2023 |
Ge L, Sinnema EG, Pérez JM, Postolache R, Castiñeira Reis M, Harutyunyan SR. Enantio- and -selective synthesis of functionalized alkenes bearing tertiary allylic stereogenic center. Science Advances. 9: eadf8742. PMID 36638168 DOI: 10.1126/sciadv.adf8742 |
0.359 |
|
| 2022 |
Somprasong S, Reis MC, Harutyunyan SR. Catalytic Access to Chiral δ-Lactams via Nucleophilic Dearomatization of Pyridine Derivatives. Angewandte Chemie (International Ed. in English). e202217328. PMID 36522289 DOI: 10.1002/anie.202217328 |
0.429 |
|
| 2022 |
Zurro M, Ge L, Harutyunyan SR. Catalytic Access to 4-(sec-Alkyl)Anilines via 1,6-Conjugate Addition of Grignard Reagents to Generated aza--Quinone Methides. Organic Letters. 24: 6686-6691. PMID 36053069 DOI: 10.1021/acs.orglett.2c02786 |
0.411 |
|
| 2022 |
Ge L, Harutyunyan SR. Manganese(i)-catalyzed access to 1,2-bisphosphine ligands. Chemical Science. 13: 1307-1312. PMID 35222914 DOI: 10.1039/d1sc06694c |
0.362 |
|
| 2022 |
Maestro A, Lemaire S, Harutyunyan SR. Cu(I)-Catalyzed Alkynylation of Quinolones. Organic Letters. 24: 1228-1231. PMID 35099185 DOI: 10.1021/acs.orglett.2c00020 |
0.66 |
|
| 2021 |
Guo Y, Castiñeira Reis M, Kootstra J, Harutyunyan SR. Enantioselective Catalytic Dearomative Addition of Grignard Reagents to 4-Methoxypyridinium Ions. Acs Catalysis. 11: 8476-8483. PMID 34306813 DOI: 10.1021/acscatal.1c01544 |
0.494 |
|
| 2020 |
Yan X, Ge L, Castiñeira Reis M, Harutyunyan SR. Nucleophilic Dearomatization of N-Heteroaromatics Enabled by Lewis Acids and Copper Catalysis. Journal of the American Chemical Society. PMID 33171043 DOI: 10.1021/jacs.0c09974 |
0.483 |
|
| 2020 |
Harutyunyan SR, Kulish K, Boldrini C, Castiñeira Reis M, Pérez J. Lewis acid promoted dearomatization of naphthols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32960476 DOI: 10.1002/Chem.202003392 |
0.392 |
|
| 2020 |
Ge L, Zurro M, Harutyunyan SR. Copper-Catalyzed Addition of Grignard Reagents to in situ Generated Indole-Derived Vinylogous Imines. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 16277-16280. PMID 32960461 DOI: 10.1002/Chem.202004232 |
0.586 |
|
| 2020 |
Guo Y, Harutyunyan SR. Copper-catalysed alkylation of heterocyclic acceptors with organometallic reagents. Beilstein Journal of Organic Chemistry. 16: 1006-1021. PMID 32509032 DOI: 10.3762/Bjoc.16.90 |
0.458 |
|
| 2019 |
Vargová D, Pérez JM, Harutyunyan SR, Šebesta R. Trapping of chiral enolates generated by Lewis acid promoted conjugate addition of Grignard reagents to unreactive Michael acceptors by various electrophiles. Chemical Communications (Cambridge, England). PMID 31513177 DOI: 10.1039/C9Cc05041H |
0.462 |
|
| 2019 |
Yan X, Harutyunyan SR. Catalytic enantioselective addition of organometallics to unprotected carboxylic acids. Nature Communications. 10: 3402. PMID 31363092 DOI: 10.1038/S41467-019-11345-Z |
0.535 |
|
| 2019 |
Guo Y, Harutyunyan SR. Highly Enantioselective Catalytic Addition of Grignard Reagents to N-Heterocyclic Acceptors. Angewandte Chemie (International Ed. in English). 58: 12950-12954. PMID 31257687 DOI: 10.1002/Anie.201906237 |
0.536 |
|
| 2019 |
Horváth A, Depré D, A Vermeulen WA, Wuyts SL, Harutyunyan SR, Binot G, Cuypers J, Couck W, Den Heuvel DV. Ring-Closing Metathesis on Commercial Scale: Synthesis of HCV Protease Inhibitor Simeprevir. The Journal of Organic Chemistry. 84: 4932-4939. PMID 30721066 DOI: 10.1021/Acs.Joc.8B03124 |
0.397 |
|
| 2019 |
Lanza F, Pérez JM, Jumde RP, Harutyunyan SR. Lewis Acid Promoted Trapping of Chiral Aza-enolates Synthesis. 51: 1253-1262. DOI: 10.1055/S-0037-1611657 |
0.476 |
|
| 2018 |
Das M, Harutyunyan S. Synergistic Action of Copper Catalysts and Lewis Acids in Carbon-Carbon Bond Forming Reactions. Chimia. 72: 642-645. PMID 30257741 DOI: 10.2533/Chimia.2018.642 |
0.727 |
|
| 2018 |
Harutyunyan SR, Guo Y, Kootstra J. Catalytic regio- and enantioselective alkylation of conjugated dienyl amides. Angewandte Chemie (International Ed. in English). PMID 30144263 DOI: 10.1002/Anie.201808392 |
0.571 |
|
| 2018 |
Collados JF, Ortiz P, Pérez JM, Xia Y, Koenis MAJ, Buma WJ, Nicu VP, Harutyunyan SR. Enantiospecific Brook Rearrangement of Tertiary Benzylic α‐Hydroxysilanes European Journal of Organic Chemistry. 2018: 3900-3903. DOI: 10.1002/Ejoc.201701469 |
0.416 |
|
| 2017 |
Jumde RP, Lanza F, Pellegrini T, Harutyunyan SR. Highly enantioselective catalytic synthesis of chiral pyridines. Nature Communications. 8: 2058. PMID 29233959 DOI: 10.1038/S41467-017-01966-7 |
0.579 |
|
| 2017 |
Rodríguez-Fernández M, Yan X, Collados JF, White PB, Harutyunyan SR. Lewis Acid Enabled Copper-Catalyzed Asymmetric Synthesis of Chiral β-Substituted Amides. Journal of the American Chemical Society. PMID 28960071 DOI: 10.1021/Jacs.7B07344 |
0.591 |
|
| 2017 |
Ortiz P, Collados JF, Jumde RP, Otten E, Harutyunyan SR. Copper-Catalyzed Enantioselective Alkylation of Enolizable Ketimines with Organomagnesium Reagents. Angewandte Chemie (International Ed. in English). PMID 28156047 DOI: 10.1002/Anie.201609963 |
0.571 |
|
| 2017 |
Hornillos V, Guduguntla S, Fañanás-Mastral M, Pérez M, Bos PH, Rudolph A, Harutyunyan SR, Feringa BL. Cu-catalyzed enantioselective allylic alkylation with organolithium reagents. Nature Protocols. 12: 493-505. PMID 28151465 DOI: 10.1038/Nprot.2016.179 |
0.533 |
|
| 2017 |
Knochel P, Ziegler D, Ortiz P, Collados JF, Jumde RP, Otten E, Harutyunyan SR. Catalytic Enantioselective Alkylation of Enolizable N-Sulfonyl Ketimines Synfacts. 13: 413-3044. DOI: 10.1055/S-0036-1590132 |
0.418 |
|
| 2016 |
Rong J, Collados JF, Ortiz P, Jumde RP, Otten E, Harutyunyan SR. Catalytic enantioselective addition of Grignard reagents to aromatic silyl ketimines. Nature Communications. 7: 13780. PMID 28008909 DOI: 10.1038/Ncomms13780 |
0.556 |
|
| 2016 |
Jumde RP, Lanza F, Veenstra MJ, Harutyunyan SR. Catalytic asymmetric addition of Grignard reagents to alkenyl-substituted aromatic N-heterocycles. Science (New York, N.Y.). 352: 433-7. PMID 27102477 DOI: 10.1126/Science.Aaf1983 |
0.568 |
|
| 2016 |
Rong J, Pellegrini T, Harutyunyan SR. Synthesis of Chiral Tertiary Alcohols by Cu(I) -Catalyzed Enantioselective Addition of Organomagnesium Reagents to Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 3558-70. PMID 26511715 DOI: 10.1002/Chem.201503412 |
0.5 |
|
| 2016 |
Collados JF, Solà R, Harutyunyan SR, Maciá B. Catalytic Synthesis of Enantiopure Chiral Alcohols via Addition of Grignard Reagents to Carbonyl Compounds Acs Catalysis. 6: 1952-1970. DOI: 10.1021/Acscatal.5B02832 |
0.457 |
|
| 2016 |
Harutyunyan SR. Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers Springer Us. DOI: 10.1007/978-3-319-33414-1 |
0.383 |
|
| 2016 |
Ortiz P, Lanza F, Harutyunyan SR. 1,2- Versus 1,4-Asymmetric Addition of Grignard Reagents to Carbonyl Compounds Topics in Organometallic Chemistry. 58: 99-134. DOI: 10.1007/3418_2015_164 |
0.446 |
|
| 2016 |
Collados JF, Ortiz P, Harutyunyan SR. On the Configurational Stability and Reactivity of Tertiary Silyloxy Carbanions Derived from Stereoselective Brook Rearrangement European Journal of Organic Chemistry. 2016: 3065-3069. DOI: 10.1002/Ejoc.201600493 |
0.425 |
|
| 2016 |
Ortiz P, Collados JF, Harutyunyan SR. Direct Synthesis of Enolizable N-Sulfonyl Ketimines under Microwave Irradiation European Journal of Organic Chemistry. 2016: 1247-1250. DOI: 10.1002/Ejoc.201600022 |
0.343 |
|
| 2016 |
Rong J, Pellegrini T, Harutyunyan SR, Šponer JE, Šponer J, Nováková O, Brabec V, Šedo O, Zdráhal Z, Costanzo G, Pino S, Saladino R, Mauro ED, Kamalov M, Kaur H, et al. Cover Picture: Synthesis of Chiral Tertiary Alcohols by CuI-Catalyzed Enantioselective Addition of Organomagnesium Reagents to Ketones / Emergence of the First Catalytic Oligonucleotides in a Formamide-Based Origin Scenario / Intermolecular Peptide Cross- Chemistry: a European Journal. 22: 3521-3521. DOI: 10.1002/Chem.201600250 |
0.437 |
|
| 2015 |
Desmarchelier A, Ortiz P, Harutyunyan SR. Tertiary α-diarylmethylamines derived from diarylketimines and organomagnesium reagents Chemical Communications. 51: 703-706. PMID 25418069 DOI: 10.1039/C4Cc06719C |
0.408 |
|
| 2015 |
Rong J, Oost R, Desmarchelier A, Minnaard AJ, Harutyunyan SR. Catalytic asymmetric alkylation of acylsilanes. Angewandte Chemie (International Ed. in English). 54: 3038-42. PMID 25403641 DOI: 10.1002/Anie.201409815 |
0.558 |
|
| 2015 |
Knochel P, Haas D, Rong G, Oost R, Desmarchelier A, Minnaard AJ, Harutyunyan SR. Asymmetric Alkylation of Acylsilanes Synfacts. 11: 189-189. DOI: 10.1055/S-0034-1379793 |
0.514 |
|
| 2015 |
Ortiz P, Del Hoyo AM, Harutyunyan SR. Catalytic asymmetric alkylation of aryl heteroaryl ketones European Journal of Organic Chemistry. 2015: 72-76. DOI: 10.1002/Ejoc.201403297 |
0.548 |
|
| 2014 |
Wu Z, Harutyunyan SR, Minnaard AJ. Total synthesis of (R,R,R)-γ-tocopherol through Cu-catalyzed asymmetric 1,2-addition. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 14250-5. PMID 25205372 DOI: 10.1002/Chem.201404458 |
0.373 |
|
| 2014 |
Rizzo A, Harutyunyan SR. Azabicycles construction: the transannular ring contraction with N-protected nucleophiles. Organic & Biomolecular Chemistry. 12: 6570-9. PMID 25007120 DOI: 10.1039/C4Ob01311E |
0.377 |
|
| 2014 |
Chen J, Lacaze E, Brasselet E, Harutyunyan SR, Katsonis N, Feringa BL. Textures of cholesteric droplets controlled by photo-switching chirality at the molecular level Journal of Materials Chemistry C. 2: 8137-8141. DOI: 10.1039/C4Tc01297F |
0.65 |
|
| 2014 |
Oost R, Rong J, Minnaard AJ, Harutyunyan SR. Synthesis of new derivatives of copper complexes of Josiphos family ligands for applications in asymmetric catalysis Catalysis Science and Technology. 4: 1997-2005. DOI: 10.1039/C4Cy00180J |
0.474 |
|
| 2014 |
Wu Z, Madduri AVR, Harutyunyan SR, Minnaard AJ. Catalytic asymmetric synthesis of dihydrofurans and cyclopentenols with tertiary stereocenters European Journal of Organic Chemistry. 2014: 575-582. DOI: 10.1002/Ejoc.201301476 |
0.508 |
|
| 2014 |
Calvo BC, Madduri AVR, Harutyunyan SR, Minnaard AJ. Copper-catalysed conjugate addition of grignard reagents to 2-methylcyclopentenone and sequential enolate alkylation Advanced Synthesis and Catalysis. 356: 2061-2069. DOI: 10.1002/Adsc.201400085 |
0.508 |
|
| 2013 |
Madduri AVR, Harutyunyan SR, Minnaard AJ. Catalytic asymmetric alkylation of ketones using organometallic reagents Drug Discovery Today: Technologies. 10: e21-e27. PMID 24050226 DOI: 10.1016/J.Ddtec.2012.10.010 |
0.469 |
|
| 2013 |
Caprioli F, Madduri AV, Minnaard AJ, Harutyunyan SR. Asymmetric amplification in the catalytic enantioselective 1,2-addition of Grignard reagents to enones. Chemical Communications (Cambridge, England). 49: 5450-2. PMID 23660758 DOI: 10.1039/C3Cc41892H |
0.533 |
|
| 2013 |
Caprioli F, Lutz M, Meetsma A, Minnaard AJ, Harutyunyan SR. Structural characterisation of Cu complexes of chiral ferrocenyl diphos-phine ligands Synlett. 24: 2419-2422. DOI: 10.1055/S-0033-1339851 |
0.362 |
|
| 2013 |
Nijland A, Harutyunyan SR. Light on the horizon? Catalytic enantioselective photoreactions Catalysis Science and Technology. 3: 1180-1189. DOI: 10.1039/C3Cy20858C |
0.465 |
|
| 2013 |
Caprioli F, Madduri AVR, Minnaard AJ, Harutyunyan SR. Asymmetric amplification in the catalytic enantioselective 1,2-addition of Grignard reagents to enones Chemical Communications. 49: 5450-5452. DOI: 10.1039/c3cc41892h |
0.496 |
|
| 2013 |
Perez M, Fananas-Mastral M, Hornillos V, Rudolph A, Bos PH, Harutyunyan SR, Feringa BL. ChemInform Abstract: Asymmetric Allylic Alkylation of Acyclic Allylic Ethers with Organolithium Reagents. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201310021 |
0.406 |
|
| 2012 |
Pérez M, Fañanás-Mastral M, Hornillos V, Rudolph A, Bos PH, Harutyunyan SR, Feringa BL. Asymmetric allylic alkylation of acyclic allylic ethers with organolithium reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 11880-3. PMID 22907628 DOI: 10.1002/Chem.201202251 |
0.627 |
|
| 2012 |
Madduri AVR, Minnaard AJ, Harutyunyan SR. Access to chiral α-bromo and α-H-substituted tertiary allylic alcohols via copper(i) catalyzed 1,2-addition of Grignard reagents to enones Organic and Biomolecular Chemistry. 10: 2878-2884. PMID 22389187 DOI: 10.1039/C2Ob25080B |
0.47 |
|
| 2012 |
Madduri AVR, Harutyunyan SR, Minnaard AJ. Asymmetric copper-catalyzed addition of grignard reagents to aryl alkyl ketones Angewandte Chemie - International Edition. 51: 3164-3167. PMID 22334477 DOI: 10.1002/Anie.201109040 |
0.535 |
|
| 2012 |
Fañanás-Mastral M, Pérez M, Bos PH, Rudolph A, Harutyunyan SR, Feringa BL. Enantioselective synthesis of tertiary and quaternary stereogenic centers: copper/phosphoramidite-catalyzed allylic alkylation with organolithium reagents. Angewandte Chemie (International Ed. in English). 51: 1922-5. PMID 22262571 DOI: 10.1002/Anie.201107840 |
0.627 |
|
| 2012 |
Bos PH, Rudolph A, Pérez M, Fañanás-Mastral M, Harutyunyan SR, Feringa BL. Copper-catalyzed asymmetric ring opening of oxabicyclic alkenes with organolithium reagents. Chemical Communications (Cambridge, England). 48: 1748-50. PMID 22215200 DOI: 10.1039/C2Cc16855C |
0.585 |
|
| 2012 |
Madduri AVR, Minnaard AJ, Harutyunyan SR. Copper(i) catalyzed asymmetric 1,2-addition of Grignard reagents to α-methyl substituted α,β-unsaturated ketones Chemical Communications. 48: 1478-1480. PMID 22124420 DOI: 10.1039/C1Cc16725A |
0.539 |
|
| 2012 |
Fananas-Mastral M, Perez M, Bos PH, Rudolph A, Harutyunyan SR, Feringa BL. ChemInform Abstract: Enantioselective Synthesis of Tertiary and Quaternary Stereogenic Centers: Copper/Phosphoramidite-Catalyzed Allylic Alkylation with Organolithium Reagents. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201227025 |
0.45 |
|
| 2011 |
Kudernac T, Ruangsupapichat N, Parschau M, Maciá B, Katsonis N, Harutyunyan SR, Ernst KH, Feringa BL. Electrically driven directional motion of a four-wheeled molecule on a metal surface. Nature. 479: 208-11. PMID 22071765 DOI: 10.1038/Nature10587 |
0.625 |
|
| 2011 |
Pérez M, Fañanás-Mastral M, Bos PH, Rudolph A, Harutyunyan SR, Feringa BL. Catalytic asymmetric carbon-carbon bond formation via allylic alkylations with organolithium compounds. Nature Chemistry. 3: 377-81. PMID 21505496 DOI: 10.1038/Nchem.1009 |
0.589 |
|
| 2011 |
Ruangsupapichat N, Pollard MM, Harutyunyan SR, Feringa BL. Reversing the direction in a light-driven rotary molecular motor. Nature Chemistry. 3: 53-60. PMID 21160518 DOI: 10.1038/Nchem.872 |
0.402 |
|
| 2011 |
Pérez M, Fañanás-Mastral M, Bos PH, Rudolph A, Harutyunyan SR, Feringa BL. Copper-Catalyzed Asymmetric Allylic Alkylation with OrganolithiumReagents Synfacts. 2011: 855-855. DOI: 10.1055/S-0030-1260817 |
0.504 |
|
| 2010 |
Kochetkov KA, Harutyunyan SR, Kuz'mina NA, Savel'eva TF, Maleev VI, Peregudov AS, Vyskocil S, Sagiyan AS. ChemInform Abstract: Asymmetric Michael Reaction of Diethyl Malonate with Crotonaldehyde Catalyzed by Chiral Aminocarboxylates, Amino Alcoholates, and Amino Phenolates. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200223032 |
0.331 |
|
| 2010 |
Belokon YN, Kochetkov KA, Churkina TD, Ikonnikov NS, Larionov OV, Harutyunyan SR, Vyskocil S, North M, Kagan HB. ChemInform Abstract: Highly Efficient Catalytic Synthesis of α-Amino Acids under Phase-Transfer Conditions with a Novel Catalyst/Substrate Pair. Cheminform. 32: no-no. DOI: 10.1002/chin.200134082 |
0.377 |
|
| 2010 |
Belokon YN, Kochetkov KA, Ikonnikov NS, Strelkova TV, Harutyunyan SR, Saghiyan AS. ChemInform Abstract: A New Synthesis of Enantiomerically Pure syn-(S)-β-Hydroxy-α-amino Acids via Asymmetric Aldol Reactions of Aldehydes with a Homochiral Ni(II)-Glycine/(S)-BPB Schiff Base Complex. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200129177 |
0.317 |
|
| 2008 |
Harutyunyan SR, den Hartog T, Geurts K, Minnaard AJ, Feringa BL. Catalytic asymmetric conjugate addition and allylic alkylation with Grignard reagents Chemical Reviews. 108: 2824-2852. PMID 18698733 DOI: 10.1021/Cr068424K |
0.804 |
|
| 2008 |
de Boer JW, Browne WR, Harutyunyan SR, Bini L, Tiemersma-Wegman TD, Alsters PL, Hage R, Feringa BL. Manganese catalysed asymmetric cis-dihydroxylation with H2O2. Chemical Communications (Cambridge, England). 3747-9. PMID 18685764 DOI: 10.1039/B808355J |
0.484 |
|
| 2008 |
Harutyunyan SR, Zhao Z, Den Hartog T, Bouwmeester K, Minnaard AJ, Feringa BL, Govers F. Biologically active Phytophthora mating hormone prepared by catalytic asymmetric total synthesis Proceedings of the National Academy of Sciences of the United States of America. 105: 8507-8512. PMID 18559862 DOI: 10.1073/Pnas.0709289105 |
0.706 |
|
| 2008 |
den Hartog T, Harutyunyan SR, Font D, Minnaard AJ, Feringa BL. Catalytic enantioselective 1,6-conjugate addition of Grignard reagents to linear dienoates. Angewandte Chemie (International Ed. in English). 47: 398-401. PMID 18041800 DOI: 10.1002/Anie.200703702 |
0.78 |
|
| 2008 |
Hartog Td, Harutyunyan SR, Font D, Minnaard AJ, Feringa BL. Copper-Catalyzed Conjugate Addition of Grignard Reagents to Dienoates Synfacts. 2008: 388-388. DOI: 10.1055/S-2008-1042788 |
0.451 |
|
| 2008 |
de Boer JW, Browne WR, Harutyunyan SR, Bini L, Tiemersma-Wegman TD, Alsters PL, Hage R, Feringa BL. ChemInform Abstract: Manganese Catalyzed Asymmetric cis-Dihydroxylation with H2O2. Cheminform. 39. DOI: 10.1002/CHIN.200852142 |
0.391 |
|
| 2008 |
Harutyunyan SR, den Hartog T, Geurts K, Minnaard AJ, Feringa BL. ChemInform Abstract: Catalytic Asymmetric Conjugated Addition and Allylic Alkylation with Grignard Reagents Cheminform. 39. DOI: 10.1002/CHIN.200848241 |
0.61 |
|
| 2008 |
den Hartog T, Harutyunyan SR, Font D, Minnaard AJ, Feringa BL. ChemInform Abstract: Catalytic Enantioselective 1,6-Conjugate Addition of Grignard Reagents to Linear Dienoates. Cheminform. 39. DOI: 10.1002/CHIN.200821030 |
0.428 |
|
| 2008 |
den Hartog T, Harutyunyan S, Font D, Minnaard A, Feringa B. Katalytische enantioselektive konjugierte 1,6-Addition von Grignard-Reagentien an lineare Dienoate Angewandte Chemie. 120: 404-407. DOI: 10.1002/Ange.200703702 |
0.408 |
|
| 2006 |
Harutyunyan SR, López F, Browne WR, Correa A, Peña D, Badorrey R, Meetsma A, Minnaard AJ, Feringa BL. On the mechanism of the copper-catalyzed enantioselective 1,4-addition of grignard reagents to alpha,beta-unsaturated carbonyl compounds. Journal of the American Chemical Society. 128: 9103-18. PMID 16834384 DOI: 10.1021/Ja0585634 |
0.61 |
|
| 2005 |
Des Mazery R, Pullez M, López F, Harutyunyan SR, Minnaard AJ, Feringa BL. An iterative catalytic route to enantiopure deoxypropionate subunits: asymmetric conjugate addition of grignard reagents to alpha,beta-unsaturated thioesters. Journal of the American Chemical Society. 127: 9966-7. PMID 16011337 DOI: 10.1021/Ja053020F |
0.505 |
|
| 2005 |
López F, Harutyunyan SR, Meetsma A, Minnaard AJ, Feringa BL. Copper-catalyzed enantioselective conjugate addition of Grignard reagents to alpha,beta-unsaturated esters. Angewandte Chemie (International Ed. in English). 44: 2752-6. PMID 15825212 DOI: 10.1002/Anie.200500317 |
0.511 |
|
| 2005 |
López F, Harutyunyan SR, Minnaard AJ, Feringa BL. Copper-catalyzed enantioselective conjugate addition of grignard reagents to acyclic enones. Journal of the American Chemical Society. 126: 12784-5. PMID 15469267 DOI: 10.1021/Ja046632T |
0.615 |
|
| 2005 |
Masery RD, Pullez M, Lopez F, Harutyunyan S, Minnaard AJ, Feringa BL. Iterative Catalytic Asymmetric Conjugate Addition to Unsaturated Thioesters Synfacts. 2005: 243-243. DOI: 10.1055/S-2005-916114 |
0.539 |
|
| 2005 |
Des Mazery R, Pullez M, Lopez F, Harutyunyan SR, Minnaard AJ, Feringa BL. An Iterative Catalytic Route to Enantiopure Deoxypropionate Subunits: Asymmetric Conjugate Addition of Grignard Reagents to α,β-Unsaturated Thioesters. Cheminform. 36. DOI: 10.1002/CHIN.200548029 |
0.421 |
|
| 2005 |
Lopez F, Harutyunyan SR, Meetsma A, Minnaard AJ, Feringa BL. Copper-Catalyzed Enantioselective Conjugate Addition of Grignard Reagents to α,β-Unsaturated Esters. Cheminform. 36. DOI: 10.1002/CHIN.200535035 |
0.454 |
|
| 2005 |
Lopez F, Harutyunyan SR, Minnaard AJ, Feringa BL. Copper-Catalyzed Enantioselective Conjugate Addition of Grignard Reagents to Acyclic Enones. Cheminform. 36. DOI: 10.1002/CHIN.200506041 |
0.557 |
|
| 2005 |
Pena D, Lopez F, Harutyunyan SR, Minnaard AJ, Feringa BL. Highly Enantioselective Cu-Catalyzed Asymmetric 1,4-Addition of Diphenylzinc to Cyclohexenone. Cheminform. 36. DOI: 10.1002/CHIN.200502090 |
0.474 |
|
| 2004 |
Michrowska A, Bujok R, Harutyunyan S, Sashuk V, Dolgonos G, Grela K. Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: enhancement of catalyst activity through electronic activation. Journal of the American Chemical Society. 126: 9318-25. PMID 15281822 DOI: 10.1021/Ja048794V |
0.75 |
|
| 2004 |
Feringa BL, Badorrey R, Peña D, Harutyunyan SR, Minnaard AJ. Copper-catalyzed asymmetric conjugate addition of Grignard reagents to cyclic enones. Proceedings of the National Academy of Sciences of the United States of America. 101: 5834-8. PMID 15075388 DOI: 10.1073/pnas.0308008101 |
0.491 |
|
| 2004 |
Feringa BL, Badorrey R, Peña D, Harutyunyan SR, Minnaard AJ. Copper-catalyzed asymmetric conjugate addition of Grignard reagents to cyclic enones Proceedings of the National Academy of Sciences of the United States of America. 101: 5834-5838. DOI: 10.1073/Pnas.0308008101 |
0.571 |
|
| 2004 |
Peña D, López F, Harutyunyan SR, Minnaard AJ, Feringa BL. Highly enantioselective Cu-catalysed asymmetric 1,4-addition of diphenylzinc to cyclohexenone Chemical Communications. 10: 1836-1837. DOI: 10.1039/B402868F |
0.511 |
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| 2004 |
Belokon YN, Harutyunyan S, Vorontsov EV, Peregudov AS, Chrustalev VN, Kochetkov KA, Pripadchev D, Sagyan AS, Beck AK, Seebach D. Nucleophilic addition to an achiral dehydroalanine Schiff Base Ni(II) complex as a route to amino acids. A case of stereodetermining asymmetric protonation in the presence of TADDOL Arkivoc. 2004: 132-150. |
0.644 |
|
| 2003 |
Belokon YN, Bespalova NB, Churkina TD, Císarová I, Ezernitskaya MG, Harutyunyan SR, Hrdina R, Kagan HB, Kocovský P, Kochetkov KA, Larionov OV, Lyssenko KA, North M, Polásek M, Peregudov AS, et al. Synthesis of alpha-amino acids via asymmetric phase transfer-catalyzed alkylation of achiral nickel(II) complexes of glycine-derived Schiff bases. Journal of the American Chemical Society. 125: 12860-71. PMID 14558835 DOI: 10.1021/Ja035465E |
0.648 |
|
| 2003 |
Grela K, Harutyunyan S, Michrowska A. A Highly Efficient Ruthenium Catalyst for Metathesis Reactions. Cheminform. 34. DOI: 10.1002/CHIN.200313060 |
0.382 |
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| 2002 |
Vyskocil S, Meca L, Tislerová I, Císarová I, Polásek M, Harutyunyan SR, Belokon YN, Stead RM, Farrugia L, Lockhart SC, Mitchell WL, Kocovský P. 2,8'-disubstituted-1,1'-binaphthyls: a new pattern in chiral ligands. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4633-48. PMID 12561104 DOI: 10.1002/1521-3765(20021018)8:20<4633::Aid-Chem4633>3.0.Co;2-N |
0.671 |
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| 2002 |
Grela K, Harutyunyan S, Michrowska A. A highly efficient ruthenium catalyst for metathesis reactions. Angewandte Chemie (International Ed. in English). 41: 4038-40. PMID 12412074 DOI: 10.1002/1521-3773(20021104)41:21<4038::Aid-Anie4038>3.0.Co;2-0 |
0.632 |
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| 2001 |
Belokon YN, Kochetkov KA, Churkina TD, Ikonnikov NS, Larionov OV, Harutyunyan SR, Vyskocil S, North M, Kagan HB. Highly Efficient Catalytic Synthesis of alpha-Amino Acids under Phase-Transfer Conditions with a Novel Catalyst/Substrate Pair This work was supported by an ISTC (grant A-356), by the Russian Foundation for Basic Research (Project No 99-03-32970), the Grant Agency of the Czech Republic (Grant No. 203/00/0601), and also by the Grant Agency of Charles University (Grant No. 18/98). We thank Prof. Pavel Kocovský for encouragement and proofreading the manuscript. Angewandte Chemie (International Ed. in English). 40: 1948-1951. PMID 11385682 DOI: 10.1002/1521-3773(20010518)40:10<1948::Aid-Anie1948>3.0.Co;2-O |
0.664 |
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| 2001 |
Belokon YN, Kochetkov KA, Ikonnikov NS, Strelkova TV, Harutyunyan SR, Saghiyan AS. A new synthesis of enantiomerically pure syn-(S)-β-hydroxy-α-amino acids via asymmetric aldol reactions of aldehydes with a homochiral Ni(II)-glycine/(S)-BPB Schiff base complex Tetrahedron Asymmetry. 12: 481-485. DOI: 10.1016/S0957-4166(01)00071-4 |
0.634 |
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