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1
An Organophilic Pervaporation Membrane Derived from Metal-Organic Framework Nanoparticles for Efficient Recovery of Bio-Alcohols
An Organophilic Pervaporation Membrane Derived from Metal-Organic Framework Nanoparticles for Efficient Recovery of Bio-Alcohols
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An Organophilic Pervaporation Membrane Derived from Metal-Organic Framework Nanoparticles for Efficient Recovery of Bio-Alcohols

Angewandte Chemie (International ed.), 2011-11, Vol.50 (45), p.10636-10639 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201104383 ;PMID: 21898739 ;CODEN: ACIEAY

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2
Catalytic Asymmetric Direct Henry Reaction of Ynals: Short Syntheses of (2S,3R)-(+)-Xestoaminol C and (-)-Codonopsinines
Catalytic Asymmetric Direct Henry Reaction of Ynals: Short Syntheses of (2S,3R)-(+)-Xestoaminol C and (-)-Codonopsinines
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Catalytic Asymmetric Direct Henry Reaction of Ynals: Short Syntheses of (2S,3R)-(+)-Xestoaminol C and (-)-Codonopsinines

Angewandte Chemie (International ed.), 2010-10, Vol.49 (41), p.7562-7565 [Peer Reviewed Journal]

Copyright © 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201004072 ;PMID: 20809559

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3
Oxygen-Mediated Coupling of Alcohols over Nanoporous Gold Catalysts at Ambient Pressures
Oxygen-Mediated Coupling of Alcohols over Nanoporous Gold Catalysts at Ambient Pressures
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Oxygen-Mediated Coupling of Alcohols over Nanoporous Gold Catalysts at Ambient Pressures

Angewandte Chemie (International ed.), 2012-02, Vol.51 (7), p.1698-1701 [Peer Reviewed Journal]

Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201107178 ;PMID: 22223430 ;CODEN: ACIEAY

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4
Acceptorless Photocatalytic Dehydrogenation for Alcohol Decarbonylation and Imine Synthesis
Acceptorless Photocatalytic Dehydrogenation for Alcohol Decarbonylation and Imine Synthesis
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Acceptorless Photocatalytic Dehydrogenation for Alcohol Decarbonylation and Imine Synthesis

Angewandte Chemie (International ed.), 2012-08, Vol.51 (34), p.8607-8610 [Peer Reviewed Journal]

Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;Copyright Wiley Subscription Services, Inc. Aug 2012 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201203556 ;PMID: 22847764 ;CODEN: ACIEAY

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5
Recent Developments in Methodology for the Direct Oxyamination of Olefins
Recent Developments in Methodology for the Direct Oxyamination of Olefins
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Recent Developments in Methodology for the Direct Oxyamination of Olefins

Chemistry : a European journal, 2011-01, Vol.17 (1), p.58-76 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.201002323 ;PMID: 21207600 ;CODEN: CEUJED

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6
Redox Self-Sufficient Biocatalyst Network for the Amination of Primary Alcohols
Redox Self-Sufficient Biocatalyst Network for the Amination of Primary Alcohols
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Redox Self-Sufficient Biocatalyst Network for the Amination of Primary Alcohols

Angewandte Chemie (International ed.), 2012-09, Vol.51 (36), p.9156-9159 [Peer Reviewed Journal]

Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201204683 ;PMID: 22887645 ;CODEN: ACIEAY

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7
Direct Catalytic Asymmetric Synthesis of anti-1,2-Amino Alcohols and syn-1,2-Diols through Organocatalytic anti-Mannich and syn-Aldol Reactions
Direct Catalytic Asymmetric Synthesis of anti-1,2-Amino Alcohols and syn-1,2-Diols through Organocatalytic anti-Mannich and syn-Aldol Reactions
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Direct Catalytic Asymmetric Synthesis of anti-1,2-Amino Alcohols and syn-1,2-Diols through Organocatalytic anti-Mannich and syn-Aldol Reactions

Journal of the American Chemical Society, 2007-01, Vol.129 (2), p.288-289 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja0677012 ;PMID: 17212404

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8
Catalyst-Free Dehydrative α-Alkylation of Ketones with Alcohols: Green and Selective Autocatalyzed Synthesis of Alcohols and Ketones
Catalyst-Free Dehydrative α-Alkylation of Ketones with Alcohols: Green and Selective Autocatalyzed Synthesis of Alcohols and Ketones
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Catalyst-Free Dehydrative α-Alkylation of Ketones with Alcohols: Green and Selective Autocatalyzed Synthesis of Alcohols and Ketones

Angewandte Chemie (International ed.), 2014-01, Vol.53 (1), p.225-229 [Peer Reviewed Journal]

Copyright © 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201308642 ;PMID: 24273002

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9
Photoredox-mediated remote C(sp 3 )-H heteroarylation of free alcohols
Photoredox-mediated remote C(sp 3 )-H heteroarylation of free alcohols
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Photoredox-mediated remote C(sp 3 )-H heteroarylation of free alcohols

Chemical science (Cambridge), 2019-01, Vol.10 (3), p.688-693 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2019 ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/c8sc04134b ;PMID: 30774869

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10
Cobalt-Catalyzed Hydrogenation of Esters to Alcohols: Unexpected Reactivity Trend Indicates Ester Enolate Intermediacy
Cobalt-Catalyzed Hydrogenation of Esters to Alcohols: Unexpected Reactivity Trend Indicates Ester Enolate Intermediacy
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Cobalt-Catalyzed Hydrogenation of Esters to Alcohols: Unexpected Reactivity Trend Indicates Ester Enolate Intermediacy

Angewandte Chemie (International ed.), 2015-10, Vol.54 (42), p.12357-12360 [Peer Reviewed Journal]

2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201502418 ;PMID: 25914240 ;CODEN: ACIEAY

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11
Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives
Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives
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Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives

Angewandte Chemie (International ed.), 2023-01, Vol.62 (4) [Peer Reviewed Journal]

ISSN: 1521-3773 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.202211952

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12
Two-Phase Dibromocyclopropanation of Unsaturated Alcohols Using Flow Chemistry
Two-Phase Dibromocyclopropanation of Unsaturated Alcohols Using Flow Chemistry
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Two-Phase Dibromocyclopropanation of Unsaturated Alcohols Using Flow Chemistry

Molecules (Basel, Switzerland), 2020-05, Vol.25 (10), p.2364 [Peer Reviewed Journal]

2020. 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. ;2020 by the authors. 2020 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules25102364 ;PMID: 32438720

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13
How Catalysts and Experimental Conditions Determine the Selective Hydroconversion of Furfural and 5-Hydroxymethylfurfural
How Catalysts and Experimental Conditions Determine the Selective Hydroconversion of Furfural and 5-Hydroxymethylfurfural
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How Catalysts and Experimental Conditions Determine the Selective Hydroconversion of Furfural and 5-Hydroxymethylfurfural

Chemical reviews, 2018-11, Vol.118 (22), p.11023-11117 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0009-2665 ;EISSN: 1520-6890 ;DOI: 10.1021/acs.chemrev.8b00134

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14
Palladium-Catalyzed Allylic Alkylation of Simple Ketones with Allylic Alcohols and Its Mechanistic Study
Palladium-Catalyzed Allylic Alkylation of Simple Ketones with Allylic Alcohols and Its Mechanistic Study
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Palladium-Catalyzed Allylic Alkylation of Simple Ketones with Allylic Alcohols and Its Mechanistic Study

Angewandte Chemie (International ed.), 2014-06, Vol.53 (26), p.6776-6780 [Peer Reviewed Journal]

2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201403410 ;PMID: 24848670 ;CODEN: ACIEAY

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15
Ethyl glucuronide concentrations in hair: a controlled alcohol-dosing study in healthy volunteers
Ethyl glucuronide concentrations in hair: a controlled alcohol-dosing study in healthy volunteers
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Ethyl glucuronide concentrations in hair: a controlled alcohol-dosing study in healthy volunteers

Analytical and bioanalytical chemistry, 2016-03, Vol.408 (8), p.2019-2025 [Peer Reviewed Journal]

Springer-Verlag Berlin Heidelberg 2015 ;COPYRIGHT 2016 Springer ;Springer-Verlag Berlin Heidelberg 2016 ;ISSN: 1618-2642 ;EISSN: 1618-2650 ;DOI: 10.1007/s00216-015-9117-0 ;PMID: 26549114

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16
Asymmetric Hydrogenation of Allylic Alcohols Using Ir-N,P-Complexes
Asymmetric Hydrogenation of Allylic Alcohols Using Ir-N,P-Complexes
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Asymmetric Hydrogenation of Allylic Alcohols Using Ir-N,P-Complexes

ACS catalysis, 2016-12, Vol.6 (12), p.8342 [Peer Reviewed Journal]

ISSN: 2155-5435 ;EISSN: 2155-5435 ;DOI: 10.1021/acscatal.6b02456

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17
An enantioselective four-component reaction via assembling two reaction intermediates
An enantioselective four-component reaction via assembling two reaction intermediates
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An enantioselective four-component reaction via assembling two reaction intermediates

Nature communications, 2022-11, Vol.13 (1), p.7088-7088, Article 7088 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-022-34913-2 ;PMID: 36400780

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18
Flexible Gold-Catalyzed Regioselective Oxidative Difunctionalization of Unactivated Alkenes
Flexible Gold-Catalyzed Regioselective Oxidative Difunctionalization of Unactivated Alkenes
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Flexible Gold-Catalyzed Regioselective Oxidative Difunctionalization of Unactivated Alkenes

Angewandte Chemie (International ed.), 2011-01, Vol.50 (4), p.906-910 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201005763 ;PMID: 21246688 ;CODEN: ACIEAY

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19
Engineered reversal of the β-oxidation cycle for the synthesis of fuels and chemicals
Engineered reversal of the β-oxidation cycle for the synthesis of fuels and chemicals
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Engineered reversal of the β-oxidation cycle for the synthesis of fuels and chemicals

Nature (London), 2011-08, Vol.476 (7360), p.355-359 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature10333 ;PMID: 21832992 ;CODEN: NATUAS

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20
Enantioselective Reduction of Ketones with "Designer Cells" at High Substrate Concentrations: Highly Efficient Access to Functionalized Optically Active Alcohols
Enantioselective Reduction of Ketones with "Designer Cells" at High Substrate Concentrations: Highly Efficient Access to Functionalized Optically Active Alcohols
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Enantioselective Reduction of Ketones with "Designer Cells" at High Substrate Concentrations: Highly Efficient Access to Functionalized Optically Active Alcohols

Angewandte Chemie (International ed.), 2006-08, Vol.45 (34), p.5677-5681 [Peer Reviewed Journal]

Copyright © 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.200503394 ;PMID: 16858704

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