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1
Computational planning of the synthesis of complex natural products
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Computational planning of the synthesis of complex natural products

Nature (London), 2020-12, Vol.588 (7836), p.83-88 [Peer Reviewed Journal]

Copyright Nature Publishing Group Dec 3, 2020 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-020-2855-y ;PMID: 33049755

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2
Natural products as inspiration for the development of asymmetric catalysis
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Natural products as inspiration for the development of asymmetric catalysis

Nature (London), 2008-09, Vol.455 (7211), p.323-332 [Peer Reviewed Journal]

COPYRIGHT 2008 Nature Publishing Group ;COPYRIGHT 2008 Nature Publishing Group ;Copyright Nature Publishing Group Sep 18, 2008 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature07370 ;PMID: 18800131 ;CODEN: NATUAS

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3
One Hundred Years of Vitamins-A Success Story of the Natural Sciences
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One Hundred Years of Vitamins-A Success Story of the Natural Sciences

Angewandte Chemie (International ed.), 2012-12, Vol.51 (52), p.12960-12990 [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.201205886 ;PMID: 23208776 ;CODEN: ACIEAY

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4
Synthesis of natural products containing spiroketals via intramolecular hydrogen abstraction
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Synthesis of natural products containing spiroketals via intramolecular hydrogen abstraction

Organic & biomolecular chemistry, 2010-01, Vol.8 (1), p.29-38 [Peer Reviewed Journal]

ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/b916041h ;PMID: 20024126

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5
Copper-catalysed selective hydroamination reactions of alkynes
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Copper-catalysed selective hydroamination reactions of alkynes

Nature chemistry, 2015-01, Vol.7 (1), p.38-44 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jan 2015 ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/nchem.2131 ;PMID: 25515888

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6
Multifunctional organoboron compounds for scalable natural product synthesis
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Multifunctional organoboron compounds for scalable natural product synthesis

Nature (London), 2014-09, Vol.513 (7518), p.367-374 [Peer Reviewed Journal]

COPYRIGHT 2014 Nature Publishing Group ;COPYRIGHT 2014 Nature Publishing Group ;Copyright Nature Publishing Group Sep 18, 2014 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature13735 ;PMID: 25230659 ;CODEN: NATUAS

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7
A platform for the discovery of new macrolide antibiotics
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A platform for the discovery of new macrolide antibiotics

Nature (London), 2016-05, Vol.533 (7603), p.338-345 [Peer Reviewed Journal]

COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group May 19, 2016 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature17967 ;PMID: 27193679 ;CODEN: NATUAS

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8
Recent Advances in the Chemical Synthesis and Evaluation of Anticancer Nucleoside Analogues
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Recent Advances in the Chemical Synthesis and Evaluation of Anticancer Nucleoside Analogues

Molecules (Basel, Switzerland), 2020-04, Vol.25 (9), p.2050 [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/molecules25092050 ;PMID: 32354007

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9
Protecting-group-free synthesis as an opportunity for invention
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Protecting-group-free synthesis as an opportunity for invention

Nature chemistry, 2009-06, Vol.1 (3), p.193-205 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2009 ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/nchem.216 ;PMID: 21378848

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10
Development of New Innovative Synthetic Organic Chemistry Using Lone Pairs of Oxygen Atoms
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Development of New Innovative Synthetic Organic Chemistry Using Lone Pairs of Oxygen Atoms

Chemical and Pharmaceutical Bulletin, 2020/10/01, Vol.68(10), pp.907-945 [Peer Reviewed Journal]

2020 The Pharmaceutical Society of Japan ;Copyright Japan Science and Technology Agency 2020 ;ISSN: 0009-2363 ;EISSN: 1347-5223 ;DOI: 10.1248/cpb.c20-00178 ;PMID: 32999145

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11
Plant Polyphenols: Chemical Properties, Biological Activities, and Synthesis
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Plant Polyphenols: Chemical Properties, Biological Activities, and Synthesis

Angewandte Chemie (International ed.), 2011-01, Vol.50 (3), p.586-621 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201000044 ;PMID: 21226137 ;CODEN: ACIEAY

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12
A Novel Class of Schistosoma mansoni Histone Deacetylase 8 (HDAC8) Inhibitors Identified by Structure-Based Virtual Screening and In Vitro Testing
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A Novel Class of Schistosoma mansoni Histone Deacetylase 8 (HDAC8) Inhibitors Identified by Structure-Based Virtual Screening and In Vitro Testing

Molecules (Basel, Switzerland), 2018-03, Vol.23 (3), p.566 [Peer Reviewed Journal]

2018. This work is licensed under https://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. ;Attribution ;2018 by the authors. 2018 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules23030566 ;PMID: 29498707

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13
Synthesis and Properties of Allenic Natural Products and Pharmaceuticals
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Synthesis and Properties of Allenic Natural Products and Pharmaceuticals

Angewandte Chemie (International ed.), 2004-02, Vol.43 (10), p.1196-1216 [Peer Reviewed Journal]

Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.200300628 ;PMID: 14991780

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14
Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry
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Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry

Current topics in medicinal chemistry, 2016-01, Vol.16 (11), p.1200-1216 [Peer Reviewed Journal]

ISSN: 1568-0266 ;EISSN: 1873-4294 ;DOI: 10.2174/1568026615666150915111741 ;PMID: 26369815

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15
The DARK Side of Total Synthesis: Strategies and Tactics in Psychoactive Drug Production
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The DARK Side of Total Synthesis: Strategies and Tactics in Psychoactive Drug Production

ACS chemical neuroscience, 2018-10, Vol.9 (10), p.2307-2330 [Peer Reviewed Journal]

ISSN: 1948-7193 ;EISSN: 1948-7193 ;DOI: 10.1021/acschemneuro.7b00528 ;PMID: 29342356

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16
Curcumin and Health
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Curcumin and Health

Molecules, 2016-02, Vol.21 (3), p.264-264 [Peer Reviewed Journal]

Copyright MDPI AG 2016 ;2016 by the authors. 2016 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules21030264 ;PMID: 26927041

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17
Direct synthesis of Z-alkenyl halides through catalytic cross-metathesis
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Direct synthesis of Z-alkenyl halides through catalytic cross-metathesis

Nature (London), 2016-03, Vol.531 (7595), p.459-465 [Peer Reviewed Journal]

COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group Mar 24, 2016 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature17396 ;PMID: 27008965 ;CODEN: NATUAS

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18
Efficient and Selective Formation of Macrocyclic Disubstituted Z Alkenes by Ring-Closing Metathesis (RCM) Reactions Catalyzed by Mo- or W-Based Monoaryloxide Pyrrolide (MAP) Complexes: Applications to Total Syntheses of Epilachnene, Yuzu Lactone, Ambrettolide, Epothilone C, and Nakadomarin A
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Efficient and Selective Formation of Macrocyclic Disubstituted Z Alkenes by Ring-Closing Metathesis (RCM) Reactions Catalyzed by Mo- or W-Based Monoaryloxide Pyrrolide (MAP) Complexes: Applications to Total Syntheses of Epilachnene, Yuzu Lactone, Ambrettolide, Epothilone C, and Nakadomarin A

Chemistry : a European journal, 2013-02, Vol.19 (8), p.2726-2740 [Peer Reviewed Journal]

Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.201204045 ;PMID: 23345004 ;CODEN: CEUJED

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19
Catalytic enantioselective synthesis of quaternary carbon stereocentres
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Article
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Catalytic enantioselective synthesis of quaternary carbon stereocentres

Nature (London), 2014-12, Vol.516 (7530), p.181-191 [Peer Reviewed Journal]

COPYRIGHT 2014 Nature Publishing Group ;COPYRIGHT 2014 Nature Publishing Group ;Copyright Nature Publishing Group Dec 11, 2014 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature14007 ;PMID: 25503231 ;CODEN: NATUAS

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20
Fight Against Antimicrobial Resistance: We Always Need New Antibacterials but for Right Bacteria
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Fight Against Antimicrobial Resistance: We Always Need New Antibacterials but for Right Bacteria

Molecules (Basel, Switzerland), 2019-08, Vol.24 (17), p.3152 [Peer Reviewed Journal]

2019. This work is licensed under https://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. ;Distributed under a Creative Commons Attribution 4.0 International License ;2019 by the authors. 2019 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules24173152 ;PMID: 31470632

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