Year |
Citation |
Score |
2022 |
Olivieri E, Shao N, Rosas R, Naubron JV, Quintard A. Catalytic Reversible (De)hydrogenation To Rotate a Chemically Fueled Molecular Switch. Angewandte Chemie (International Ed. in English). e202214763. PMID 36226997 DOI: 10.1002/anie.202214763 |
0.745 |
|
2022 |
Shao N, Rodriguez J, Quintard A. Catalysis Driven Six-Step Synthesis of Apratoxin A Key Polyketide Fragment. Organic Letters. 24: 6537-6542. PMID 36073851 DOI: 10.1021/acs.orglett.2c02482 |
0.671 |
|
2022 |
Olivieri E, Gasch B, Quintard G, Naubron JV, Quintard A. Dissipative Acid-Fueled Reprogrammable Supramolecular Materials. Acs Applied Materials & Interfaces. 14: 24720-24728. PMID 35580903 DOI: 10.1021/acsami.2c01608 |
0.614 |
|
2022 |
Thomas A, Gasch B, Olivieri E, Quintard A. Trichloroacetic acid fueled practical amine purifications. Beilstein Journal of Organic Chemistry. 18: 225-231. PMID 35280955 DOI: 10.3762/bjoc.18.26 |
0.749 |
|
2021 |
Shao N, Liu X, Monnier V, Charles L, Rodriguez J, Bressy C, Quintard A. Enantioselective Synthesis of Acyclic Stereotriads Featuring Fluorinated Tetrasubstituted Stereocenters. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34821417 DOI: 10.1002/chem.202103874 |
0.8 |
|
2021 |
Bressy C, Quintard A, Médebielle M, Desrues T, Merad J, Andrei D, Pons JM, Parrain JL. Impact of the Difluoromethylene Group (CF2) in Organocatalyzed Acylative Kinetic Resolution of α,α-Difluorohydrins. Angewandte Chemie (International Ed. in English). PMID 34473886 DOI: 10.1002/anie.202107041 |
0.716 |
|
2021 |
Olivieri E, Quintard G, Naubron JV, Quintard A. Chemically Fueled Three-State Chiroptical Switching Supramolecular Gel with Temporal Control. Journal of the American Chemical Society. 143: 12650-12657. PMID 34351739 DOI: 10.1021/jacs.1c05183 |
0.639 |
|
2021 |
Yagoub I, Clémancey M, Bayle PA, Quintard A, Delattre G, Blondin G, Kochem A. Mössbauer Spectroscopic and Computational Investigation of An Iron Cyclopentadienone Complex. Inorganic Chemistry. PMID 34264639 DOI: 10.1021/acs.inorgchem.1c01155 |
0.324 |
|
2021 |
Yagoub I, Clémancey M, Bayle PA, Quintard A, Delattre G, Blondin G, Kochem A. Mössbauer Spectroscopic and Computational Investigation of An Iron Cyclopentadienone Complex. Inorganic Chemistry. PMID 34264639 DOI: 10.1021/acs.inorgchem.1c01155 |
0.324 |
|
2021 |
Desrues T, Liu X, Pons JM, Monnier V, Amalian JA, Charles L, Quintard A, Bressy C. Indirect Tertiary Alcohol Enantiocontrol by Acylative Organocatalytic Kinetic Resolution. Organic Letters. PMID 33999644 DOI: 10.1021/acs.orglett.1c01261 |
0.708 |
|
2021 |
Desrues T, Liu X, Pons JM, Monnier V, Amalian JA, Charles L, Quintard A, Bressy C. Indirect Tertiary Alcohol Enantiocontrol by Acylative Organocatalytic Kinetic Resolution. Organic Letters. PMID 33999644 DOI: 10.1021/acs.orglett.1c01261 |
0.708 |
|
2021 |
Quintard A. Copper Catalyzed Decarboxylative Functionalization of Ketoacids. Chemical Record (New York, N.Y.). PMID 33750015 DOI: 10.1002/tcr.202100045 |
0.353 |
|
2021 |
Quintard A. Copper Catalyzed Decarboxylative Functionalization of Ketoacids. Chemical Record (New York, N.Y.). PMID 33750015 DOI: 10.1002/tcr.202100045 |
0.353 |
|
2020 |
Shao N, Rodriguez J, Quintard A. Redox-Neutral 1,3-Diol Synthesis by Base-Promoted Diastereoselective Alcohol-Aldolization. Organic Letters. PMID 32877190 DOI: 10.1021/Acs.Orglett.0C02536 |
0.656 |
|
2020 |
Shao N, Rodriguez J, Quintard A. Redox-Neutral 1,3-Diol Synthesis by Base-Promoted Diastereoselective Alcohol-Aldolization. Organic Letters. PMID 32877190 DOI: 10.1021/Acs.Orglett.0C02536 |
0.656 |
|
2020 |
Sperandio C, Rodriguez J, Quintard A. Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1,3,5-triols featuring supramolecular recognition properties. Chemical Science. 11: 1629-1635. PMID 32206281 DOI: 10.1039/C9Sc05196A |
0.824 |
|
2020 |
Sperandio C, Rodriguez J, Quintard A. Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1,3,5-triols featuring supramolecular recognition properties. Chemical Science. 11: 1629-1635. PMID 32206281 DOI: 10.1039/C9Sc05196A |
0.824 |
|
2020 |
Sperandio C, Rodriguez J, Quintard A. Organocatalytic carbon dioxide fixation to epoxides by perfluorinated 1,3,5-triols catalysts. Organic & Biomolecular Chemistry. PMID 32196062 DOI: 10.1039/D0Ob00402B |
0.791 |
|
2020 |
Sperandio C, Rodriguez J, Quintard A. Organocatalytic carbon dioxide fixation to epoxides by perfluorinated 1,3,5-triols catalysts. Organic & Biomolecular Chemistry. PMID 32196062 DOI: 10.1039/D0Ob00402B |
0.791 |
|
2020 |
Sperandio C, Rodriguez J, Quintard A. Catalytic strategies towards 1,3-polyol synthesis by enantioselective cascades creating multiple alcohol functions. Organic & Biomolecular Chemistry. PMID 31976499 DOI: 10.1039/C9Ob02675D |
0.82 |
|
2020 |
Sperandio C, Rodriguez J, Quintard A. Catalytic strategies towards 1,3-polyol synthesis by enantioselective cascades creating multiple alcohol functions. Organic & Biomolecular Chemistry. PMID 31976499 DOI: 10.1039/C9Ob02675D |
0.82 |
|
2020 |
Sperandio C, Rodriguez J, Quintard A. Three‐component multi‐catalytic enantioselective oxa‐Michael/aldolization sequence and application to (+)‐yashabushitriol synthesis European Journal of Organic Chemistry. 2020: 2493-2496. DOI: 10.1002/Ejoc.202000185 |
0.773 |
|
2019 |
Sperandio C, Quintard G, Naubron JV, Giorgi M, Yemloul M, Parrain JL, Rodriguez J, Quintard A. Strategic stereoselective halogen insertion (F, Cl), a tool to enhance supramolecular properties in polyols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31453654 DOI: 10.1002/Chem.201902983 |
0.767 |
|
2019 |
Sperandio C, Quintard G, Naubron JV, Giorgi M, Yemloul M, Parrain JL, Rodriguez J, Quintard A. Strategic stereoselective halogen insertion (F, Cl), a tool to enhance supramolecular properties in polyols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31453654 DOI: 10.1002/Chem.201902983 |
0.767 |
|
2018 |
Quintard A, Rodriguez J. Enantioselective Ir-Catalyzed Bidirectional Reductive Coupling. Organic Letters. PMID 30592423 DOI: 10.1021/Acs.Orglett.8B03669 |
0.394 |
|
2018 |
Rodriguez J, Quintard A. Discovery of Eco-compatible Synthetic Paths by a Multi-catalysis Approach. Chimia. 72: 580-583. PMID 30257730 DOI: 10.2533/Chimia.2018.580 |
0.413 |
|
2018 |
Quintard A, Sperandio C, Rodriguez J. Modular Enantioselective Synthesis of an Advanced Pentahydroxy Intermediate of Antimalarial Bastimolide A and of Fluorinated and Chlorinated Analogues. Organic Letters. PMID 30129767 DOI: 10.1021/Acs.Orglett.8B02213 |
0.802 |
|
2018 |
Quintard A, Sperandio C, Rodriguez J. Modular Enantioselective Synthesis of an Advanced Pentahydroxy Intermediate of Antimalarial Bastimolide A and of Fluorinated and Chlorinated Analogues. Organic Letters. PMID 30129767 DOI: 10.1021/Acs.Orglett.8B02213 |
0.802 |
|
2017 |
Quintard A, Rodriguez J. Organocatalytic Activation of Diethyl Glutaconate for the Diastereo- and Enantioselective Assembly of NH-Free 2,3,4-Trisubstituted Pyrrolidines. Organic Letters. PMID 28124924 DOI: 10.1021/Acs.Orglett.7B00014 |
0.333 |
|
2017 |
Quintard A, Roudier M, Rodriguez J. Multicatalytic Enantioselective Borrowing Hydrogen δ-Lactonization Strategy from β-Keto Esters and Allylic Alcohols Synthesis. 50: 785-792. DOI: 10.1055/S-0036-1588547 |
0.341 |
|
2017 |
Quintard A, Rodriguez J. Bicatalyzed Three-Component Stereoselective Decarboxylative Fluoro-Aldolization for the Construction of Elongated Fluorohydrins Acs Catalysis. 7: 5513-5517. DOI: 10.1021/Acscatal.7B02353 |
0.357 |
|
2016 |
Quintard A, Rodriguez J. Catalytic enantioselective OFF ↔ ON activation processes initiated by hydrogen transfer: concepts and challenges. Chemical Communications (Cambridge, England). PMID 27381644 DOI: 10.1039/C6Cc03486A |
0.327 |
|
2016 |
Roudier M, Constantieux T, Rodriguez J, Quintard A. Recent Achievements in Enantioselective Borrowing Hydrogen by the Combination of Iron- and Organocatalysis. Chimia. 70: 97-101. PMID 26931224 DOI: 10.2533/Chimia.2016.97 |
0.633 |
|
2016 |
Roudier M, Constantieux T, Rodriguez J, Quintard A. Recent Achievements in Enantioselective Borrowing Hydrogen by the Combination of Iron- and Organocatalysis. Chimia. 70: 97-101. PMID 26931224 DOI: 10.2533/Chimia.2016.97 |
0.633 |
|
2016 |
Roudier M, Constantieux T, Quintard A, Rodriguez J. Triple Iron/Copper/Iminium Activation for the Efficient Redox Neutral Catalytic Enantioselective Functionalization of Allylic Alcohols Acs Catalysis. 6: 5236-5244. DOI: 10.1021/Acscatal.6B01102 |
0.354 |
|
2015 |
Quintard A, Rodriguez J. A Step into an eco-Compatible Future: Iron- and Cobalt-catalyzed Borrowing Hydrogen Transformation. Chemsuschem. PMID 26666210 DOI: 10.1002/Cssc.201501460 |
0.326 |
|
2015 |
Quintard A, Rodriguez J. Didecarboxylative Iron-Catalyzed Bidirectional Aldolization towards Diversity-Oriented Ketodiol Synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 14717-22. PMID 26332439 DOI: 10.1002/Chem.201502788 |
0.325 |
|
2015 |
Quintard A, Rodriguez J. Synergistic Cu-amine catalysis for the enantioselective synthesis of chiral cyclohexenones. Chemical Communications. 51: 9523-9526. PMID 25968341 DOI: 10.1039/C5Cc02987B |
0.373 |
|
2015 |
Roudier M, Constantieux T, Quintard A, Rodriguez J. Enantioselective Synthesis of Medium‐Sized‐Ring Lactones by Organocatalytic Michael Addition Followed by Reductively Initiated Fragmentation European Journal of Organic Chemistry. 2015: 5709-5711. DOI: 10.1002/Ejoc.201500894 |
0.317 |
|
2014 |
Roudier M, Constantieux T, Quintard A, Rodriguez J. Enantioselective cascade formal reductive insertion of allylic alcohols into the C(O)-C bond of 1,3-diketones: ready access to synthetically valuable 3-alkylpentanol units. Organic Letters. 16: 2802-5. PMID 24849709 DOI: 10.1021/Ol500821C |
0.631 |
|
2014 |
Roudier M, Constantieux T, Quintard A, Rodriguez J. Enantioselective cascade formal reductive insertion of allylic alcohols into the C(O)-C bond of 1,3-diketones: ready access to synthetically valuable 3-alkylpentanol units. Organic Letters. 16: 2802-5. PMID 24849709 DOI: 10.1021/Ol500821C |
0.631 |
|
2013 |
Quintard A, Constantieux T, Rodriguez J. An iron/amine-catalyzed cascade process for the enantioselective functionalization of allylic alcohols. Angewandte Chemie (International Ed. in English). 52: 12883-7. PMID 24130036 DOI: 10.1002/Anie.201307295 |
0.322 |
|
2013 |
Bugaut X, Bonne D, Raimondi W, Sanchez Duque M, Goudedranche S, Quintard A, Constantieux T, Rodriguez J. Activation of 1,2- and 1,3-Ketoamides with Thiourea Organocatalyst for the Enantioselective Domino Synthesis of Functionalized Cyclohexanes Synthesis. 45: 1659-1666. DOI: 10.1055/S-0033-1338844 |
0.356 |
|
2012 |
Trost BM, Quintard A. Asymmetric catalytic synthesis of the proposed structure of trocheliophorolide B. Organic Letters. 14: 4698-700. PMID 22913543 DOI: 10.1021/Ol302074H |
0.427 |
|
2012 |
Trost BM, Quintard A. Asymmetric catalytic synthesis of the proposed structure of trocheliophorolide B. Organic Letters. 14: 4698-700. PMID 22913543 DOI: 10.1021/Ol302074H |
0.427 |
|
2012 |
Trost BM, Quintard A. Asymmetric catalytic alkynylation of acetaldehyde: application to the synthesis of (+)-tetrahydropyrenophorol. Angewandte Chemie (International Ed. in English). 51: 6704-8. PMID 22674869 DOI: 10.1002/Anie.201203035 |
0.482 |
|
2012 |
Trost BM, Quintard A. Asymmetric catalytic alkynylation of acetaldehyde: application to the synthesis of (+)-tetrahydropyrenophorol. Angewandte Chemie (International Ed. in English). 51: 6704-8. PMID 22674869 DOI: 10.1002/Anie.201203035 |
0.482 |
|
2012 |
Trost BM, Quintard A. ChemInform Abstract: Asymmetric Catalytic Synthesis of the Proposed Structure of Trocheliophorolide B. Cheminform. 43: no-no. DOI: 10.1002/chin.201252169 |
0.376 |
|
2012 |
Trost BM, Quintard A. ChemInform Abstract: Asymmetric Catalytic Alkynylation of Acetaldehyde: Application to the Synthesis of (+)-Tetrahydropyrenophorol. Cheminform. 43: no-no. DOI: 10.1002/chin.201246042 |
0.478 |
|
2011 |
Quintard A, Langlois JB, Emery D, Mareda J, Guénée L, Alexakis A. Conformationally stabilized catalysts by fluorine insertion: tool for enantioselectivity improvement. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13433-7. PMID 22038655 DOI: 10.1002/Chem.201102757 |
0.528 |
|
2011 |
Quintard A, Langlois JB, Emery D, Mareda J, Guénée L, Alexakis A. Conformationally stabilized catalysts by fluorine insertion: tool for enantioselectivity improvement. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13433-7. PMID 22038655 DOI: 10.1002/Chem.201102757 |
0.528 |
|
2011 |
Quintard A, Alexakis A. Highly enantioselective organocascade intermolecular iminium/enamine Michael addition on enals Chemical Communications. 47: 7212-7214. PMID 21603716 DOI: 10.1039/C1Cc11967B |
0.538 |
|
2011 |
Quintard A, Alexakis A. Highly enantioselective organocascade intermolecular iminium/enamine Michael addition on enals Chemical Communications. 47: 7212-7214. PMID 21603716 DOI: 10.1039/C1Cc11967B |
0.538 |
|
2011 |
Murphy JJ, Quintard A, McArdle P, Alexakis A, Stephens JC. Asymmetric organocatalytic 1,6-conjugate addition of aldehydes to dienic sulfones. Angewandte Chemie (International Ed. in English). 50: 5095-8. PMID 21538747 DOI: 10.1002/Anie.201100804 |
0.504 |
|
2011 |
Murphy JJ, Quintard A, McArdle P, Alexakis A, Stephens JC. Asymmetric organocatalytic 1,6-conjugate addition of aldehydes to dienic sulfones. Angewandte Chemie (International Ed. in English). 50: 5095-8. PMID 21538747 DOI: 10.1002/Anie.201100804 |
0.504 |
|
2011 |
Quintard A, Alexakis A, Mazet C. Access to high levels of molecular complexity by one-pot iridium/enamine asymmetric catalysis. Angewandte Chemie (International Ed. in English). 50: 2354-8. PMID 21351353 DOI: 10.1002/Anie.201007001 |
0.597 |
|
2011 |
Quintard A, Alexakis A, Mazet C. Access to high levels of molecular complexity by one-pot iridium/enamine asymmetric catalysis. Angewandte Chemie (International Ed. in English). 50: 2354-8. PMID 21351353 DOI: 10.1002/Anie.201007001 |
0.597 |
|
2011 |
Quintard A, Lefranc A, Alexakis A. Highly enantioselective direct vinylogous Michael addition of γ-butenolide to enals Organic Letters. 13: 1540-1543. PMID 21319834 DOI: 10.1021/Ol200235J |
0.579 |
|
2011 |
Quintard A, Lefranc A, Alexakis A. Highly enantioselective direct vinylogous Michael addition of γ-butenolide to enals Organic Letters. 13: 1540-1543. PMID 21319834 DOI: 10.1021/Ol200235J |
0.579 |
|
2011 |
Quintard A, Alexakis A. 1,2-Sulfone rearrangement in organocatalytic reactions. Organic & Biomolecular Chemistry. 9: 1407-18. PMID 21212902 DOI: 10.1039/c0ob00818d |
0.576 |
|
2011 |
Quintard A, Alexakis A. 1,2-Sulfone rearrangement in organocatalytic reactions. Organic & Biomolecular Chemistry. 9: 1407-18. PMID 21212902 DOI: 10.1039/c0ob00818d |
0.576 |
|
2011 |
Murphy JJ, Quintard A, McArdle P, Alexakis A, Stephens JC. Dienic Sulfones as Efficient 1,6-Acceptors in the Additionof Aldehydes Synfacts. 2011: 788-788. DOI: 10.1055/S-0030-1260631 |
0.472 |
|
2011 |
Quintard A, Alexakis A, Mazet C. One-Pot Iridium and Enamine Catalysis Synfacts. 2011: 519-519. DOI: 10.1055/S-0030-1259834 |
0.571 |
|
2011 |
Quintard A, Alexakis A. 1,2-Sulfone rearrangement in organocatalytic reactions Organic and Biomolecular Chemistry. 9: 1407-1418. DOI: 10.1039/C0Ob00818D |
0.576 |
|
2011 |
Quintard A, Alexakis A, Mazet C. Access to high levels of molecular complexity by one-pot iridium/enamine asymmetric catalysis Angewandte Chemie - International Edition. 50: 2354-2358. DOI: 10.1002/anie.201007001 |
0.593 |
|
2010 |
Quintard A, Alexakis A. Asymmetric addition of alpha-hetero-disubstituted aldehydes to vinyl sulfones; formation of highly functionalized tetrasubstituted carbon centres. Chemical Communications (Cambridge, England). 46: 4085-7. PMID 20401408 DOI: 10.1039/c000326c |
0.497 |
|
2010 |
Quintard A, Alexakis A. Asymmetric addition of alpha-hetero-disubstituted aldehydes to vinyl sulfones; formation of highly functionalized tetrasubstituted carbon centres. Chemical Communications (Cambridge, England). 46: 4085-7. PMID 20401408 DOI: 10.1039/c000326c |
0.497 |
|
2010 |
Palais L, Babel L, Quintard A, Belot S, Alexakis A. Copper-catalyzed enantioselective 1,4-addition to alpha,beta-unsaturated aldehydes. Organic Letters. 12: 1988-91. PMID 20359170 DOI: 10.1021/ol100441r |
0.496 |
|
2010 |
Palais L, Babel L, Quintard A, Belot S, Alexakis A. Copper-catalyzed enantioselective 1,4-addition to alpha,beta-unsaturated aldehydes. Organic Letters. 12: 1988-91. PMID 20359170 DOI: 10.1021/ol100441r |
0.496 |
|
2010 |
Quintard A, Alexakis A. Asymmetric addition of α-hetero-disubstituted aldehydes to vinyl sulfones; Formation of highly functionalized tetrasubstituted carbon centres Chemical Communications. 46: 4085-4087. DOI: 10.1039/C000326C |
0.542 |
|
2010 |
Palais L, Babel L, Quintard A, Belot S, Alexakis A. Copper-catalyzed enantioselective 1,4-addition to α,β- unsaturated aldehydes Organic Letters. 12: 1988-1991. DOI: 10.1021/Ol100441R |
0.507 |
|
2010 |
Bournaud C, Marchal E, Quintard A, Sulzer-Mossé S, Alexakis A. Organocatalyst-mediated enantioselective intramolecular Michael addition of aldehydes to vinyl sulfones Tetrahedron Asymmetry. 21: 1666-1673. DOI: 10.1016/J.Tetasy.2010.03.043 |
0.556 |
|
2010 |
Quintard A, Belot S, Marchai E, Alexakis A. Aminal-pyrrolidine organocatalysts - Highly efficient and modular catalysts for α-functionalization of carbonyl compounds European Journal of Organic Chemistry. 927-936. DOI: 10.1002/Ejoc.200901283 |
0.535 |
|
2010 |
Palais L, Babel L, Quintard A, Belot S, Alexakis A. ChemInform Abstract: Copper-Catalyzed Enantioselective 1,4-Addition to α,β-Unsaturated Aldehydes. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201038070 |
0.452 |
|
2010 |
Belot S, Quintard A, Krause N, Alexakis A. ChemInform Abstract: Organocatalyzed Conjugate Addition of Carbonyl Compounds to Nitrodienes/Nitroenynes and Synthetic Applications. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201028044 |
0.429 |
|
2010 |
Quintard A, Alexakis A. Highly enantioselective one-pot copper-catalyzed 1,4 addition/ organocatalyzed α-substitution of enals Advanced Synthesis and Catalysis. 352: 1856-1860. DOI: 10.1002/Adsc.201000309 |
0.538 |
|
2010 |
Belot S, Quintard A, Krause N, Alexakis A. Organocatalyzed conjugate addition of carbonyl compounds to nitrodienes/nitroenynes and synthetic applications Advanced Synthesis and Catalysis. 352: 667-695. DOI: 10.1002/Adsc.200900814 |
0.626 |
|
2009 |
Quintard A, Alexakis A. Organocatalytic addition on 1,2-bis(sulfone)vinylenes leading to an unprecedented rearrangement. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11109-13. PMID 19777516 DOI: 10.1002/chem.200901535 |
0.502 |
|
2009 |
Quintard A, Alexakis A. Organocatalytic addition on 1,2-bis(sulfone)vinylenes leading to an unprecedented rearrangement. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11109-13. PMID 19777516 DOI: 10.1002/chem.200901535 |
0.502 |
|
2009 |
Quintard A, Alexakis A. Organocatalytic addition on l,2-bis(sulfone)vinylenes leading to an unprecedented rearrangement Chemistry - a European Journal. 15: 11109-11113. DOI: 10.1002/Chem.200901535 |
0.538 |
|
2008 |
Quintard A, Bournaud C, Alexakis A. Diversity-oriented synthesis towards conceptually new highly modular aminal-pyrrolidine organocatalysts Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 7504-7507. PMID 18666273 DOI: 10.1002/Chem.200801212 |
0.566 |
|
2008 |
Quintard A, Bournaud C, Alexakis A. Diversity-oriented synthesis towards conceptually new highly modular aminal-pyrrolidine organocatalysts Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 7504-7507. PMID 18666273 DOI: 10.1002/Chem.200801212 |
0.566 |
|
2007 |
Quintard A, Darbost U, Vocanson F, Pellet-Rostaing S, Lemaire M. Synthesis of new calix[4]arene based chiral ligands bearing β-amino alcohol groups and their application in asymmetric transfer hydrogenation Tetrahedron-Asymmetry. 18: 1926-1933. DOI: 10.1016/J.Tetasy.2007.07.018 |
0.33 |
|
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