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Results 1 - 20 of 2,938,802  for All Library Resources

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1
Catalytic functionalization of unactivated primary C-H bonds directed by an alcohol
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Article
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Catalytic functionalization of unactivated primary C-H bonds directed by an alcohol

Nature (London), 2012-02, Vol.483 (7387), p.70-73 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Mar 1, 2012 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature10785 ;PMID: 22382981 ;CODEN: NATUAS

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2
Electronic Structure of Bis(imino)pyridine Iron Dichloride, Monochloride, and Neutral Ligand Complexes:  A Combined Structural, Spectroscopic, and Computational Study
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Electronic Structure of Bis(imino)pyridine Iron Dichloride, Monochloride, and Neutral Ligand Complexes:  A Combined Structural, Spectroscopic, and Computational Study

Journal of the American Chemical Society, 2006-10, Vol.128 (42), p.13901-13912 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja064557b ;PMID: 17044718 ;CODEN: JACSAT

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3
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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4
Photon Gated Transport at the Glass Nanopore Electrode
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Photon Gated Transport at the Glass Nanopore Electrode

Journal of the American Chemical Society, 2006-10, Vol.128 (41), p.13553-13558 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja064274j ;PMID: 17031969 ;CODEN: JACSAT

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5
Collective synthesis of natural products by means of organocascade catalysis
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Article
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Collective synthesis of natural products by means of organocascade catalysis

Nature (London), 2011-07, Vol.475 (7355), p.183-188 [Peer Reviewed Journal]

2015 INIST-CNRS ;2011 Macmillan Publishers Limited. All rights reserved ;Copyright Nature Publishing Group Jul 14, 2011 ;2011 Macmillan Publishers Limited. All rights reserved 2011 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature10232 ;PMID: 21753848 ;CODEN: NATUAS

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6
Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway
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Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway

Journal of organic chemistry, 2008-07, Vol.73 (14), p.5520-5528 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/jo800733p ;PMID: 18557650 ;CODEN: JOCEAH

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7
Ligand Redox Effects in the Synthesis, Electronic Structure, and Reactivity of an Alkyl−Alkyl Cross-Coupling Catalyst
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Article
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Ligand Redox Effects in the Synthesis, Electronic Structure, and Reactivity of an Alkyl−Alkyl Cross-Coupling Catalyst

Journal of the American Chemical Society, 2006-10, Vol.128 (40), p.13175-13183 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja063334i ;PMID: 17017797 ;CODEN: JACSAT

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8
Catalysis of Diribonucleoside Monophosphate Cleavage by Water Soluble Copper(II) Complexes of Calix[4]arene Based Nitrogen Ligands
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Article
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Catalysis of Diribonucleoside Monophosphate Cleavage by Water Soluble Copper(II) Complexes of Calix[4]arene Based Nitrogen Ligands

Journal of the American Chemical Society, 2006-09, Vol.128 (37), p.12322-12330 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja0632106 ;PMID: 16967984 ;CODEN: JACSAT

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9
Well-Defined Chiral Spiro Iridium/Phosphine−Oxazoline Cationic Complexes for Highly Enantioselective Hydrogenation of Imines at Ambient Pressure
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Article
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Well-Defined Chiral Spiro Iridium/Phosphine−Oxazoline Cationic Complexes for Highly Enantioselective Hydrogenation of Imines at Ambient Pressure

Journal of the American Chemical Society, 2006-10, Vol.128 (39), p.12886-12891 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja063444p ;PMID: 17002383 ;CODEN: JACSAT

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10
Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles
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Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles

Journal of organic chemistry, 2008-05, Vol.73 (9), p.3475-3480 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo702692a ;PMID: 18376862 ;CODEN: JOCEAH

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11
CF3 Oxonium Salts, O-(Trifluoromethyl)dibenzofuranium Salts:  In Situ Synthesis, Properties, and Application as a Real CF3 + Species Reagent
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Article
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CF3 Oxonium Salts, O-(Trifluoromethyl)dibenzofuranium Salts:  In Situ Synthesis, Properties, and Application as a Real CF3 + Species Reagent

Journal of organic chemistry, 2007-08, Vol.72 (18), p.6905-6917 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo070896r ;PMID: 17676906 ;CODEN: JOCEAH

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12
N-Heterocyclic Carbenes in Transition Metal Catalysis and Organocatalysis
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Book
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N-Heterocyclic Carbenes in Transition Metal Catalysis and Organocatalysis

Springer Science+Business Media B.V. 2011 ;ISSN: 0920-4652 ;ISBN: 9048128668 ;ISBN: 9789048128662 ;ISBN: 904812865X ;ISBN: 9789048128655 ;EISBN: 9048128668 ;EISBN: 9789048128662 ;DOI: 10.1007/978-90-481-2866-2 ;OCLC: 704395339

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13
Sequence-Specific Recognition and Cooperative Dimerization of N-Terminal Aromatic Peptides in Aqueous Solution by a Synthetic Host
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Sequence-Specific Recognition and Cooperative Dimerization of N-Terminal Aromatic Peptides in Aqueous Solution by a Synthetic Host

Journal of the American Chemical Society, 2006-09, Vol.128 (38), p.12574-12581 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja064323s ;PMID: 16984208 ;CODEN: JACSAT

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14
Parallel Synthesis of a Library of Benzoxazoles and Benzothiazoles Using Ligand-Accelerated Copper-Catalyzed Cyclizations of ortho-Halobenzanilides
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Article
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Parallel Synthesis of a Library of Benzoxazoles and Benzothiazoles Using Ligand-Accelerated Copper-Catalyzed Cyclizations of ortho-Halobenzanilides

Journal of organic chemistry, 2006-03, Vol.71 (5), p.1802-1808 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo051927q ;PMID: 16496964 ;CODEN: JOCEAH

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15
Lewis Acid-Catalyzed Enantioselective Hydroxylation Reactions of Oxindoles and β-Keto Esters Using DBFOX Ligand
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Article
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Lewis Acid-Catalyzed Enantioselective Hydroxylation Reactions of Oxindoles and β-Keto Esters Using DBFOX Ligand

Journal of the American Chemical Society, 2006-12, Vol.128 (51), p.16488-16489 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja0668825 ;PMID: 17177383 ;CODEN: JACSAT

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16
The Selective Reaction of Aryl Halides with KOH:  Synthesis of Phenols, Aromatic Ethers, and Benzofurans
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Article
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The Selective Reaction of Aryl Halides with KOH:  Synthesis of Phenols, Aromatic Ethers, and Benzofurans

Journal of the American Chemical Society, 2006-08, Vol.128 (33), p.10694-10695 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja0639719 ;PMID: 16910660 ;CODEN: JACSAT

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17
Synthesis of macrocyclic natural products by catalyst-controlled stereoselective ring-closing metathesis
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Synthesis of macrocyclic natural products by catalyst-controlled stereoselective ring-closing metathesis

Nature (London), 2011-11, Vol.479 (7371), p.88-93 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Nov 3, 2011 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature10563 ;PMID: 22051677 ;CODEN: NATUAS

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18
Experimental and Computational Study of a Liquid Crystalline Dimesogen Exhibiting Nematic, Twist-Bend Nematic, Intercalated Smectic, and Soft Crystalline Mesophases
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Experimental and Computational Study of a Liquid Crystalline Dimesogen Exhibiting Nematic, Twist-Bend Nematic, Intercalated Smectic, and Soft Crystalline Mesophases

Molecules (Basel, Switzerland), 2021-01, Vol.26 (3), p.532 [Peer Reviewed Journal]

2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules26030532 ;PMID: 33498518

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19
Heterocyclic Anticancer Compounds: Recent Advances and the Paradigm Shift towards the Use of Nanomedicine's Tool Box
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Article
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Heterocyclic Anticancer Compounds: Recent Advances and the Paradigm Shift towards the Use of Nanomedicine's Tool Box

Molecules, 2015-09, Vol.20 (9), p.16852-16891 [Peer Reviewed Journal]

Copyright MDPI AG 2015 ;2015 by the authors. 2015 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules200916852 ;PMID: 26389876

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20
Lessons from Nature: Biomimetic Organocatalytic Carbon−Carbon Bond Formations
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Lessons from Nature: Biomimetic Organocatalytic Carbon−Carbon Bond Formations

Journal of organic chemistry, 2008-10, Vol.73 (20), p.7857-7870 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo801374j ;PMID: 18778100 ;CODEN: JOCEAH

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