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1
Understanding the Reactivity of Captodative Ethylenes in Polar Cycloaddition Reactions. A Theoretical Study
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Understanding the Reactivity of Captodative Ethylenes in Polar Cycloaddition Reactions. A Theoretical Study

Journal of organic chemistry, 2008-06, Vol.73 (12), p.4615-4624 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo800572a ;PMID: 18484771 ;CODEN: JOCEAH

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2
Molecular Electron Density Theory: A Modern View of Reactivity in Organic Chemistry
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Molecular Electron Density Theory: A Modern View of Reactivity in Organic Chemistry

Molecules (Basel, Switzerland), 2016-09, Vol.21 (10), p.1319 [Peer Reviewed Journal]

Copyright MDPI AG 2016 ;2016 by the authors. 2016 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules21101319 ;PMID: 27706053

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3
Overcoming lability of extremely long alkane carbon―carbon bonds through dispersion forces
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Overcoming lability of extremely long alkane carbon―carbon bonds through dispersion forces

Nature (London), 2011-09, Vol.477 (7364), p.308-311 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Sep 15, 2011 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature10367 ;PMID: 21921913 ;CODEN: NATUAS

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4
Nucleus-Independent Chemical Shifts (NICS):  Distance Dependence and Revised Criteria for Aromaticity and Antiaromaticity
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Nucleus-Independent Chemical Shifts (NICS):  Distance Dependence and Revised Criteria for Aromaticity and Antiaromaticity

Journal of organic chemistry, 2006-02, Vol.71 (3), p.883-893 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo051746o ;PMID: 16438497 ;CODEN: JOCEAH

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5
A graph-convolutional neural network model for the prediction of chemical reactivity
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A graph-convolutional neural network model for the prediction of chemical reactivity

Chemical science (Cambridge), 2019-01, Vol.10 (2), p.370-377 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2019 ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/c8sc04228d ;PMID: 30746086

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6
Practical and innate carbon―hydrogen functionalization of heterocycles
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Practical and innate carbon―hydrogen functionalization of heterocycles

Nature (London), 2012-12, Vol.492 (7427), p.95-99 [Peer Reviewed Journal]

2014 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Dec 6, 2012 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature11680 ;PMID: 23201691 ;CODEN: NATUAS

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7
N-Heterocyclic Carbene-Catalyzed Generation of Homoenolates:  γ-Butyrolactones by Direct Annulations of Enals and Aldehydes
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N-Heterocyclic Carbene-Catalyzed Generation of Homoenolates:  γ-Butyrolactones by Direct Annulations of Enals and Aldehydes

Journal of the American Chemical Society, 2004-11, Vol.126 (44), p.14370-14371 [Peer Reviewed Journal]

Copyright © 2004 American Chemical Society ;2005 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja044714b ;PMID: 15521753 ;CODEN: JACSAT

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8
Activation of remote meta―C―H bonds assisted by an end-on template
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Activation of remote meta―C―H bonds assisted by an end-on template

Nature (London), 2012-06, Vol.486 (7404), p.518-522 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Jun 28, 2012 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature11158 ;PMID: 22739317 ;CODEN: NATUAS

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9
C2-Symmetric Bicyclo[2.2.2]octadienes as Chiral Ligands:  Their High Performance in Rhodium-Catalyzed Asymmetric Arylation of N-Tosylarylimines
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C2-Symmetric Bicyclo[2.2.2]octadienes as Chiral Ligands:  Their High Performance in Rhodium-Catalyzed Asymmetric Arylation of N-Tosylarylimines

Journal of the American Chemical Society, 2004-10, Vol.126 (42), p.13584-13585 [Peer Reviewed Journal]

2005 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja044790e ;PMID: 15493893 ;CODEN: JACSAT

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10
Exploiting Acyl and Enol Azolium Intermediates via N-Heterocyclic Carbene-Catalyzed Reactions of α-Reducible Aldehydes
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Exploiting Acyl and Enol Azolium Intermediates via N-Heterocyclic Carbene-Catalyzed Reactions of α-Reducible Aldehydes

Advanced synthesis & catalysis, 2012-06, Vol.354 (9), p.1617-1639 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.201200031

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11
Sterically Demanding, Bioxazoline-Derived N-Heterocyclic Carbene Ligands with Restricted Flexibility for Catalysis
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Sterically Demanding, Bioxazoline-Derived N-Heterocyclic Carbene Ligands with Restricted Flexibility for Catalysis

Journal of the American Chemical Society, 2004-11, Vol.126 (46), p.15195-15201 [Peer Reviewed Journal]

Copyright © 2004 American Chemical Society ;2005 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja045349r ;PMID: 15548016 ;CODEN: JACSAT

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12
A Highly Efficient Organocatalyst for Direct Aldol Reactions of Ketones with Aldedydes
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A Highly Efficient Organocatalyst for Direct Aldol Reactions of Ketones with Aldedydes

Journal of the American Chemical Society, 2005-06, Vol.127 (25), p.9285-9289 [Peer Reviewed Journal]

Copyright © 2005 American Chemical Society ;2005 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja0510156 ;CODEN: JACSAT

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13
When Organocatalysis Meets Transition-Metal Catalysis
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When Organocatalysis Meets Transition-Metal Catalysis

European Journal of Organic Chemistry, 2010-06, Vol.2010 (16), p.2999-3025 [Peer Reviewed Journal]

Copyright © 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 INIST-CNRS ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.201000004

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14
α-Functionalization of carbonyl compounds using hypervalent iodine reagents
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α-Functionalization of carbonyl compounds using hypervalent iodine reagents

Synthesis (Stuttgart), 2011-02 (4), p.517 [Peer Reviewed Journal]

ISSN: 1437-210X ;ISSN: 0039-7881 ;EISSN: 1437-210X ;DOI: 10.1055/s-0030-1258328

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15
The Enantioselective Tsuji Allylation
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The Enantioselective Tsuji Allylation

Journal of the American Chemical Society, 2004-11, Vol.126 (46), p.15044-15045 [Peer Reviewed Journal]

Copyright © 2004 American Chemical Society ;2005 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja044812x ;PMID: 15547998 ;CODEN: JACSAT

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16
Thiourea-Catalyzed Asymmetric Michael Addition of Activated Methylene Compounds to α,β-Unsaturated Imides:  Dual Activation of Imide by Intra- and Intermolecular Hydrogen Bonding
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Thiourea-Catalyzed Asymmetric Michael Addition of Activated Methylene Compounds to α,β-Unsaturated Imides:  Dual Activation of Imide by Intra- and Intermolecular Hydrogen Bonding

Journal of the American Chemical Society, 2006-07, Vol.128 (29), p.9413-9419 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja061364f ;PMID: 16848477 ;CODEN: JACSAT

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17
A RuH2(CO)(PPh3)3-Catalyzed Regioselective Arylation of Aromatic Ketones with Arylboronates via Carbon−Hydrogen Bond Cleavage
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A RuH2(CO)(PPh3)3-Catalyzed Regioselective Arylation of Aromatic Ketones with Arylboronates via Carbon−Hydrogen Bond Cleavage

Journal of the American Chemical Society, 2005-04, Vol.127 (16), p.5936-5945 [Peer Reviewed Journal]

Copyright © 2005 American Chemical Society ;2005 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja043334n ;CODEN: JACSAT

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18
Catalytic Asymmetric Synthesis of Piperidine Derivatives through the [4 + 2] Annulation of Imines with Allenes
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Catalytic Asymmetric Synthesis of Piperidine Derivatives through the [4 + 2] Annulation of Imines with Allenes

Journal of the American Chemical Society, 2005-09, Vol.127 (35), p.12234-12235 [Peer Reviewed Journal]

Copyright © 2005 American Chemical Society ;2005 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja053277d ;PMID: 16131196 ;CODEN: JACSAT

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19
Vitrimers: directing chemical reactivity to control material properties
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Vitrimers: directing chemical reactivity to control material properties

Chemical science (Cambridge), 2020-04, Vol.11 (19), p.4855-487 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2020 ;Distributed under a Creative Commons Attribution 4.0 International License ;This journal is © The Royal Society of Chemistry 2020 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d0sc01069c ;PMID: 34122941

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20
Enhancing the potential of enantioselective organocatalysis with light
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Enhancing the potential of enantioselective organocatalysis with light

Nature (London), 2018-02, Vol.554 (7690), p.41-49 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Feb 1, 2018 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature25175 ;PMID: 29388950

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