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1
Comparing the Performances of Force Fields in Conformational Searching of Hydrogen-Bond-Donating Catalysts
Comparing the Performances of Force Fields in Conformational Searching of Hydrogen-Bond-Donating Catalysts
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Comparing the Performances of Force Fields in Conformational Searching of Hydrogen-Bond-Donating Catalysts

Journal of Organic Chemistry, 2022-05, Vol.87 (9) [Peer Reviewed Journal]

Publisher Copyright: © 2022 The Authors. ;ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.2c00066

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2
Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones
Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones
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Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones

Journal of Organic Chemistry, 2022-03, Vol.87 (5), p.3482-3490 [Peer Reviewed Journal]

Publisher Copyright: © 2022 American Chemical Society. All rights reserved. ;ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.1c03045 ;PMID: 35179890

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3
The Saegusa Oxidation and Related Procedures
The Saegusa Oxidation and Related Procedures
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The Saegusa Oxidation and Related Procedures

Distributed under a Creative Commons Attribution 4.0 International License ;DOI: 10.1002/0471264180.or098.01

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4
Azulene functionalization by iron-mediated addition to a cyclohexadiene scaffold
Azulene functionalization by iron-mediated addition to a cyclohexadiene scaffold
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Azulene functionalization by iron-mediated addition to a cyclohexadiene scaffold

Journal of Organic Chemistry, 2020-11, Vol.85 (21), p.13453-13465 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.0c01412

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5
C4-aldehyde of guaiazulene: synthesis and derivatisation
C4-aldehyde of guaiazulene: synthesis and derivatisation
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C4-aldehyde of guaiazulene: synthesis and derivatisation

Organic and Biomolecular Chemistry, 2021-03, Vol.19 (11), p.2502-2511 [Peer Reviewed Journal]

Publisher Copyright: © The Royal Society of Chemistry 2021. Copyright: Copyright 2021 Elsevier B.V., All rights reserved. ;ISSN: 1477-0520 ;ISSN: 1477-0539 ;EISSN: 1477-0539 ;DOI: 10.1039/d0ob02567d ;PMID: 33661271

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6
Use of ArSO 2 SR f reagents: an efficient tool for the introduction of SR f moieties
Use of ArSO 2 SR f reagents: an efficient tool for the introduction of SR f moieties
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Use of ArSO 2 SR f reagents: an efficient tool for the introduction of SR f moieties

Organic & biomolecular chemistry, 2019-02, Vol.17 (7), p.1683-1693 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/c8ob02995d

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7
Publisher’s Note: “Thermodynamics of chemical waves” [J. Chem. Phys. 151, 234103 (2019)]
Publisher’s Note: “Thermodynamics of chemical waves” [J. Chem. Phys. 151, 234103 (2019)]
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Publisher’s Note: “Thermodynamics of chemical waves” [J. Chem. Phys. 151, 234103 (2019)]

The Journal of chemical physics, 2020-01, Vol.152 (3), p.039901-039901 [Peer Reviewed Journal]

Author(s) ;2020 Author(s). Published under license by AIP Publishing. ;ISSN: 0021-9606 ;EISSN: 1089-7690 ;DOI: 10.1063/1.5143654 ;PMID: 31968972 ;CODEN: JCPSA6

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8
Publisher’s Note: “Chemical and hydrodynamic alignment of an enzyme” [J. Chem. Phys. 150, 115102 (2019)]
Publisher’s Note: “Chemical and hydrodynamic alignment of an enzyme” [J. Chem. Phys. 150, 115102 (2019)]
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Publisher’s Note: “Chemical and hydrodynamic alignment of an enzyme” [J. Chem. Phys. 150, 115102 (2019)]

The Journal of chemical physics, 2019-04, Vol.150 (15), p.159903-159903 [Peer Reviewed Journal]

Author(s) ;ISSN: 0021-9606 ;EISSN: 1089-7690 ;DOI: 10.1063/1.5097948 ;PMID: 31005068 ;CODEN: JCPSA6

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9
Selective Activation of Chalcogen Bonding: An Efficient Structuring Tool toward Crystal Engineering Strategies
Selective Activation of Chalcogen Bonding: An Efficient Structuring Tool toward Crystal Engineering Strategies
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Selective Activation of Chalcogen Bonding: An Efficient Structuring Tool toward Crystal Engineering Strategies

Accounts of chemical research, 2024-02, Vol.57 (3), p.362-374 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0001-4842 ;EISSN: 1520-4898 ;DOI: 10.1021/acs.accounts.3c00674 ;PMID: 38275221

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10
Synthesis of Terminal Ribose Analogues of Adenosine 5′-Diphosphate Ribose as Probes for the Transient Receptor Potential Cation Channel TRPM2
Synthesis of Terminal Ribose Analogues of Adenosine 5′-Diphosphate Ribose as Probes for the Transient Receptor Potential Cation Channel TRPM2
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Synthesis of Terminal Ribose Analogues of Adenosine 5′-Diphosphate Ribose as Probes for the Transient Receptor Potential Cation Channel TRPM2

Journal of Organic Chemistry, 2019-05, Vol.84 (10), p.6143-6157 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.9b00338 ;PMID: 30978018

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11
Electronic Decoupling in C3-Symmetrical Light-Responsive Tris(Azobenzene) Scaffolds: Self-Assembly and Multiphotochromism
Electronic Decoupling in C3-Symmetrical Light-Responsive Tris(Azobenzene) Scaffolds: Self-Assembly and Multiphotochromism
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Electronic Decoupling in C3-Symmetrical Light-Responsive Tris(Azobenzene) Scaffolds: Self-Assembly and Multiphotochromism

Journal of the American Chemical Society, 2018-11, Vol.140 (47), p.16062-16070 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b06324

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12
Assembly of Divalent Ligands and Their Effect on Divalent Binding to Pseudomonas aeruginosa Lectin LecA
Assembly of Divalent Ligands and Their Effect on Divalent Binding to Pseudomonas aeruginosa Lectin LecA
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Assembly of Divalent Ligands and Their Effect on Divalent Binding to Pseudomonas aeruginosa Lectin LecA

info:eu-repo/semantics/OpenAccess ;ISSN: 0022-3263 ;EISSN: 1520-6904

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13
Amendments: Author Correction: ClampFISH detects individual nucleic acid molecules using click chemistry-based amplification
Amendments: Author Correction: ClampFISH detects individual nucleic acid molecules using click chemistry-based amplification
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Amendments: Author Correction: ClampFISH detects individual nucleic acid molecules using click chemistry-based amplification

Nature biotechnology, 2019-01, Vol.37 (1), p.102-102 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Jan 2019 ;ISSN: 1087-0156 ;EISSN: 1546-1696 ;DOI: 10.1038/nbt0119-102b ;PMID: 30605160

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14
Proline-Based Boronic Acid Receptors for Chiral Recognition of Glucose
Proline-Based Boronic Acid Receptors for Chiral Recognition of Glucose
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Proline-Based Boronic Acid Receptors for Chiral Recognition of Glucose

Journal of Organic Chemistry, 2018-12, Vol.83 (24), p.15128-15135 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.8b02425 ;PMID: 30465430

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15
Experimental and Theoretical Study of the Kinetics of the CH 3 + HBr → CH 4 + Br Reaction and the Temperature Dependence of the Activation Energy of CH 4 + Br → CH 3 + HBr
Experimental and Theoretical Study of the Kinetics of the CH 3 + HBr → CH 4 + Br Reaction and the Temperature Dependence of the Activation Energy of CH 4 + Br → CH 3 + HBr
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Experimental and Theoretical Study of the Kinetics of the CH 3 + HBr → CH 4 + Br Reaction and the Temperature Dependence of the Activation Energy of CH 4 + Br → CH 3 + HBr

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2023-08, Vol.127 (33), p.6916-6923 [Peer Reviewed Journal]

Attribution ;ISSN: 1089-5639 ;EISSN: 1520-5215 ;DOI: 10.1021/acs.jpca.3c03685

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16
Mechanistic Insights into a Chiral Phosphoric Acid-Catalyzed Asymmetric Pinacol Rearrangement
Mechanistic Insights into a Chiral Phosphoric Acid-Catalyzed Asymmetric Pinacol Rearrangement
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Mechanistic Insights into a Chiral Phosphoric Acid-Catalyzed Asymmetric Pinacol Rearrangement

Journal of Organic Chemistry, 2018-12, Vol.83 (23), p.14683-14687 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.8b02812

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17
Publisher Correction: The role of reticular chemistry in the design of CO2 reduction catalysts
Publisher Correction: The role of reticular chemistry in the design of CO2 reduction catalysts
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Publisher Correction: The role of reticular chemistry in the design of CO2 reduction catalysts

Nature materials, 2018-10, Vol.17 (10), p.943-943 [Peer Reviewed Journal]

Copyright Nature Publishing Group Oct 2018 ;ISSN: 1476-1122 ;EISSN: 1476-4660 ;DOI: 10.1038/s41563-018-0159-5

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18
Publisher Correction: Unexpected intersystem crossing
Publisher Correction: Unexpected intersystem crossing
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Publisher Correction: Unexpected intersystem crossing

Nature chemistry, 2019-03, Vol.11 (3), p.278-278 [Peer Reviewed Journal]

2019© Springer Nature Limited 2019 ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/s41557-019-0229-6 ;PMID: 30733571

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19
Chemistry of Strigolactones, Key Players in Plant Communication
Chemistry of Strigolactones, Key Players in Plant Communication
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Chemistry of Strigolactones, Key Players in Plant Communication

Chembiochem : a European journal of chemical biology, 2024-04 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1439-4227 ;EISSN: 1439-7633 ;DOI: 10.1002/cbic.202400133

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20
Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis
Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis
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Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis

Journal of organic chemistry, 2022-05, Vol.87 (9), p.5690-5702 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.2c00054

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