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1
An Autonomous Self-Optimizing Flow Reactor for the Synthesis of Natural Product Carpanone
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An Autonomous Self-Optimizing Flow Reactor for the Synthesis of Natural Product Carpanone

Journal of organic chemistry, 2018-12, Vol.83 (23), p.14286-14299 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.8b01821

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2
Developing a Highly Active Catalytic System Based on Cobalt Nanoparticles for Terminal and Internal Alkene Hydrosilylation
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Developing a Highly Active Catalytic System Based on Cobalt Nanoparticles for Terminal and Internal Alkene Hydrosilylation

Journal of organic chemistry, 2020-09, Vol.85 (18), p.11732-11740 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.0c01439

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3
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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4
Mild and Highly Efficient Method for the Synthesis of 2-Arylbenzimidazoles and 2-Arylbenzothiazoles
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Mild and Highly Efficient Method for the Synthesis of 2-Arylbenzimidazoles and 2-Arylbenzothiazoles

Journal of organic chemistry, 2008-09, Vol.73 (17), p.6835-6837 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo8010232 ;PMID: 18652508 ;CODEN: JOCEAH

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5
Aerobic Oxidative EDA Catalysis: Synthesis of Tetrahydroquinolines Using an Organocatalytic EDA Active Acceptor
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Aerobic Oxidative EDA Catalysis: Synthesis of Tetrahydroquinolines Using an Organocatalytic EDA Active Acceptor

Journal of organic chemistry, 2022-01, Vol.87 (2), p.1457 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.1c02776

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6
Tuning the HOMO and LUMO Energy Levels of Organic Chromophores for Dye Sensitized Solar Cells
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Article
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Tuning the HOMO and LUMO Energy Levels of Organic Chromophores for Dye Sensitized Solar Cells

Journal of organic chemistry, 2007-12, Vol.72 (25), p.9550-9556 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/jo701592x ;PMID: 17979286 ;CODEN: JOCEAH

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7
Extension of the Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile to a Full Span of 28 pKa Units:  Unification of Different Basicity Scales
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Extension of the Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile to a Full Span of 28 pKa Units:  Unification of Different Basicity Scales

Journal of organic chemistry, 2005-02, Vol.70 (3), p.1019-1028 [Peer Reviewed Journal]

2005 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo048252w ;PMID: 15675863 ;CODEN: JOCEAH

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8
Nonthermal Microwave Effects Revisited:  On the Importance of Internal Temperature Monitoring and Agitation in Microwave Chemistry
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Nonthermal Microwave Effects Revisited:  On the Importance of Internal Temperature Monitoring and Agitation in Microwave Chemistry

Journal of organic chemistry, 2008-01, Vol.73 (1), p.36-47 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo7022697 ;PMID: 18062704 ;CODEN: JOCEAH

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9
Visible-Light-Driven Stereoselective Annulation of Alkyl Anilines and Dibenzoylethylenes via Electron Donor-Acceptor Complexes
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Visible-Light-Driven Stereoselective Annulation of Alkyl Anilines and Dibenzoylethylenes via Electron Donor-Acceptor Complexes

Journal of organic chemistry, 2021-01, Vol.86 (2), p.1901 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.0c02819

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10
1,4-D-Sorbitan: A Promising Biobased-Platform for the Synthesis of Chiral Amines
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1,4-D-Sorbitan: A Promising Biobased-Platform for the Synthesis of Chiral Amines

Journal of organic chemistry, 2023-02 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.2c02827

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11
Mechanochemical Preparation of Hydantoins from Amino Esters: Application to the Synthesis of the Antiepileptic Drug Phenytoin
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Mechanochemical Preparation of Hydantoins from Amino Esters: Application to the Synthesis of the Antiepileptic Drug Phenytoin

Journal of organic chemistry, 2014-11, Vol.79 (21), p.10132-10142 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo5017629

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12
The Art of Building Small:  From Molecular Switches to Molecular Motors
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The Art of Building Small:  From Molecular Switches to Molecular Motors

Journal of organic chemistry, 2007-08, Vol.72 (18), p.6635-6652 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo070394d ;PMID: 17629332 ;CODEN: JOCEAH

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13
One-Pot Synthesis of Unsymmetric Diaryliodonium Salts from Iodine and Arenes
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One-Pot Synthesis of Unsymmetric Diaryliodonium Salts from Iodine and Arenes

Journal of organic chemistry, 2017-11, Vol.82 (22), p.11909 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.7b01652

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14
Trifluoromethylthiolation, Trifluoromethylation, and Arylation Reactions of Difluoro Enol Silyl Ethers
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Article
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Trifluoromethylthiolation, Trifluoromethylation, and Arylation Reactions of Difluoro Enol Silyl Ethers

Journal of organic chemistry, 2020-07, Vol.85 (13), p.8311 [Peer Reviewed Journal]

ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.0c01030

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15
Starburst Triarylamine Based Dyes for Efficient Dye-Sensitized Solar Cells
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Starburst Triarylamine Based Dyes for Efficient Dye-Sensitized Solar Cells

Journal of organic chemistry, 2008-05, Vol.73 (10), p.3791-3797 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/jo800159t ;PMID: 18412319 ;CODEN: JOCEAH

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16
Intramolecular Pd(II)-Catalyzed Oxidative Biaryl Synthesis Under Air: Reaction Development and Scope
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Article
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Intramolecular Pd(II)-Catalyzed Oxidative Biaryl Synthesis Under Air: Reaction Development and Scope

Journal of organic chemistry, 2008-07, Vol.73 (13), p.5022-5028 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo800596m ;PMID: 18543991 ;CODEN: JOCEAH

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17
Determination of the Rate Constant of the [4 + 2] Cycloaddition Between an Aryne Atropisomer and Furan in Solution
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Determination of the Rate Constant of the [4 + 2] Cycloaddition Between an Aryne Atropisomer and Furan in Solution

Journal of organic chemistry, 2022-08, Vol.87 (16), p.11141-11147 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.2c01394 ;PMID: 35946800

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18
Amino Acid Promoted CuI-Catalyzed C−N Bond Formation between Aryl Halides and Amines or N-Containing Heterocycles
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Article
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Amino Acid Promoted CuI-Catalyzed C−N Bond Formation between Aryl Halides and Amines or N-Containing Heterocycles

Journal of organic chemistry, 2005-06, Vol.70 (13), p.5164-5173 [Peer Reviewed Journal]

Copyright © 2005 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo0504464 ;PMID: 15960520 ;CODEN: JOCEAH

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19
Structural Diversity of Organic Chemistry. A Scaffold Analysis of the CAS Registry
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Article
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Structural Diversity of Organic Chemistry. A Scaffold Analysis of the CAS Registry

Journal of organic chemistry, 2008-06, Vol.73 (12), p.4443-4451 [Peer Reviewed Journal]

2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo8001276 ;PMID: 18505297 ;CODEN: JOCEAH

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20
Helical Chirality Induces a Substrate-Selectivity Switch in Carbohydrates Recognitions
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Article
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Helical Chirality Induces a Substrate-Selectivity Switch in Carbohydrates Recognitions

Journal of organic chemistry, 2018-06, Vol.83 (12), p.6301-6306 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.8b00276

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