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1
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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2
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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3
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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4
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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5
Glycosyl ortho-(1-phenylvinyl)benzoates versatile glycosyl donors for highly efficient synthesis of both O-glycosides and nucleosides
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Glycosyl ortho-(1-phenylvinyl)benzoates versatile glycosyl donors for highly efficient synthesis of both O-glycosides and nucleosides

Nature communications, 2020-01, Vol.11 (1), p.405-10, Article 405 [Peer Reviewed Journal]

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) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-14295-z ;PMID: 31964883

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6
Catalytic enantioselective synthesis of quaternary carbon stereocentres
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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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7
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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8
Tetrazolium compounds: synthesis and applications in medicine
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Article
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Tetrazolium compounds: synthesis and applications in medicine

Molecules, 2015-03, Vol.20 (4), p.5528-5553 [Peer Reviewed Journal]

Copyright MDPI AG 2015 ;2015 by the authors. 2015 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules20045528 ;PMID: 25826789

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9
Bioactive Thiazine and Benzothiazine Derivatives: Green Synthesis Methods and Their Medicinal Importance
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Bioactive Thiazine and Benzothiazine Derivatives: Green Synthesis Methods and Their Medicinal Importance

Molecules (Basel, Switzerland), 2016-08, Vol.21 (8), p.1054 [Peer Reviewed Journal]

2016 by the authors. 2016 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules21081054 ;PMID: 27537865

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10
Total synthesis of bryostatin 16 using atom-economical and chemoselective approaches
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Total synthesis of bryostatin 16 using atom-economical and chemoselective approaches

Nature, 2008-11, Vol.456 (7221), p.485-488 [Peer Reviewed Journal]

2009 INIST-CNRS ;COPYRIGHT 2008 Nature Publishing Group ;COPYRIGHT 2008 Nature Publishing Group ;Copyright Nature Publishing Group Nov 27, 2008 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;EISSN: 1476-4679 ;DOI: 10.1038/nature07543 ;PMID: 19037312 ;CODEN: NATUAS

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11
A Review on Biological Activities and Chemical Synthesis of Hydrazide Derivatives
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Article
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A Review on Biological Activities and Chemical Synthesis of Hydrazide Derivatives

Current medicinal chemistry, 2012-02, Vol.19 (4), p.569-612 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0929-8673 ;EISSN: 1875-533X ;DOI: 10.2174/092986712798918789 ;PMID: 22204327

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12
Nucleobase synthesis in interstellar ices
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Article
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Nucleobase synthesis in interstellar ices

Nature communications, 2019-09, Vol.10 (1), p.4413-8, Article 4413 [Peer Reviewed Journal]

2019. 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) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-12404-1 ;PMID: 31562325

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13
Recent Advances in Efficient and Selective Synthesis of Di-, Tri-, and Tetrasubstituted Alkenes via Pd-Catalyzed Alkenylation−Carbonyl Olefination Synergy
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Recent Advances in Efficient and Selective Synthesis of Di-, Tri-, and Tetrasubstituted Alkenes via Pd-Catalyzed Alkenylation−Carbonyl Olefination Synergy

Accounts of chemical research, 2008-11, Vol.41 (11), p.1474-1485 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;ISSN: 0001-4842 ;EISSN: 1520-4898 ;DOI: 10.1021/ar800038e ;PMID: 18783256

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14
Diverse compounds from pleuromutilin lead to a thioredoxin inhibitor and inducer of ferroptosis
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Article
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Diverse compounds from pleuromutilin lead to a thioredoxin inhibitor and inducer of ferroptosis

Nature chemistry, 2019-06, Vol.11 (6), p.521-532 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Nature Limited 2019. ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/s41557-019-0261-6 ;PMID: 31086302

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15
Recent Advances in the Chemistry and Biology of Benzothiazoles
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Article
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Recent Advances in the Chemistry and Biology of Benzothiazoles

Archiv der Pharmazie (Weinheim), 2015-03, Vol.348 (3), p.155-178 [Peer Reviewed Journal]

2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 0365-6233 ;EISSN: 1521-4184 ;DOI: 10.1002/ardp.201400340 ;PMID: 25682746

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16
Evolution of multi-component anion relay chemistry (ARC): construction of architecturally complex natural and unnatural products
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Article
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Evolution of multi-component anion relay chemistry (ARC): construction of architecturally complex natural and unnatural products

Chemical communications (Cambridge, England), 2008-01 (45), p.5883-5895 [Peer Reviewed Journal]

ISSN: 1359-7345 ;EISSN: 1364-548X ;DOI: 10.1039/b810394a ;PMID: 19030533

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17
Nineteen-step total synthesis of (+)-phorbol
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Article
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Nineteen-step total synthesis of (+)-phorbol

Nature (London), 2016-04, Vol.532 (7597), p.90-93 [Peer Reviewed Journal]

COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group Apr 7, 2016 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature17153 ;PMID: 27007853 ;CODEN: NATUAS

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18
Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review
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Article
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Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review

Molecules (Basel, Switzerland), 2017-03, Vol.22 (3), p.387 [Peer Reviewed Journal]

Copyright MDPI AG 2017 ;2017 by the authors. 2017 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules22030387 ;PMID: 28257115

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19
Biocatalytic retrosynthesis
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Article
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Biocatalytic retrosynthesis

Nature chemical biology, 2013-05, Vol.9 (5), p.285-288 [Peer Reviewed Journal]

Copyright Nature Publishing Group May 2013 ;ISSN: 1552-4450 ;EISSN: 1552-4469 ;DOI: 10.1038/nchembio.1235 ;PMID: 23594772

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20
Catalytic Z-selective olefin cross-metathesis for natural product synthesis
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Catalytic Z-selective olefin cross-metathesis for natural product synthesis

Nature (London), 2011-03, Vol.471 (7339), p.461-466 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Mar 24, 2011 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature09957 ;PMID: 21430774 ;CODEN: NATUAS

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