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1
A catalytic alkene insertion approach to bicyclo[2.1.1]hexane bioisosteres
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A catalytic alkene insertion approach to bicyclo[2.1.1]hexane bioisosteres

Nature chemistry, 2023-04, Vol.15 (4), p.535-541 [Peer Reviewed Journal]

2023. The Author(s), under exclusive licence to Springer Nature Limited. ;The Author(s), under exclusive licence to Springer Nature Limited 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/s41557-023-01135-y ;PMID: 36781910

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2
1,2-Disubstituted bicyclo[2.1.1]hexanes as saturated bioisosteres of ortho -substituted benzene
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1,2-Disubstituted bicyclo[2.1.1]hexanes as saturated bioisosteres of ortho -substituted benzene

Chemical science (Cambridge), 2023-12, Vol.14 (48), p.14092-14099 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2023 ;This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d3sc05121h ;PMID: 38098705

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3
2,5-disubstituted bicyclo[2.1.1]hexanes as rigidified cyclopentane variants
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2,5-disubstituted bicyclo[2.1.1]hexanes as rigidified cyclopentane variants

Chemical science (Cambridge), 2023-08, Vol.14 (3), p.87-875 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2023 ;This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d3sc02695g ;PMID: 37538817

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4
A palladium-catalyzed cyclization-oxidation sequence: synthesis of bicyclo[3.1.0]hexanes and evidence for S(N)2 C-O bond formation
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A palladium-catalyzed cyclization-oxidation sequence: synthesis of bicyclo[3.1.0]hexanes and evidence for S(N)2 C-O bond formation

Journal of the American Chemical Society, 2007-04, Vol.129 (16), p.4906-4907 [Peer Reviewed Journal]

ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja070919j ;PMID: 17394326

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5
Synthesis of polysubstituted bicyclo[2.1.1]hexanes enabling access to new chemical space
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Article
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Synthesis of polysubstituted bicyclo[2.1.1]hexanes enabling access to new chemical space

Chemical science (Cambridge), 2023-09, Vol.14 (36), p.9885-9891 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2023 ;This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d3sc03083k

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6
Stepwise reduction of a base-stabilised ferrocenyl aluminium() dihalide for the synthesis of structurally-diverse dialane species
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Article
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Stepwise reduction of a base-stabilised ferrocenyl aluminium() dihalide for the synthesis of structurally-diverse dialane species

Chemical science (Cambridge), 2022-08, Vol.13 (33), p.9693-97 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2022 ;This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d2sc02783f ;PMID: 36091914

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7
Catalytic undirected borylation of tertiary C-H bonds in bicyclo[1.1.1]pentanes and bicyclo[2.1.1]hexanes
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Catalytic undirected borylation of tertiary C-H bonds in bicyclo[1.1.1]pentanes and bicyclo[2.1.1]hexanes

Nature chemistry, 2023-05, Vol.15 (5), p.685-693 [Peer Reviewed Journal]

2023. The Author(s), under exclusive licence to Springer Nature Limited. ;The Author(s), under exclusive licence to Springer Nature Limited 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/s41557-023-01159-4 ;PMID: 36973434

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8
A Complete Separation of Hexane Isomers by a Functionalized Flexible Metal Organic Framework
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A Complete Separation of Hexane Isomers by a Functionalized Flexible Metal Organic Framework

Advanced functional materials, 2014-12, Vol.24 (48), p.7666-7673 [Peer Reviewed Journal]

2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1616-301X ;EISSN: 1616-3028 ;DOI: 10.1002/adfm.201401974

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9
Synthesis of bicyclo[3.1.0]hexanes by (3 + 2) annulation of cyclopropenes with aminocyclopropanes
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Synthesis of bicyclo[3.1.0]hexanes by (3 + 2) annulation of cyclopropenes with aminocyclopropanes

Chemical science (Cambridge), 2019-12, Vol.1 (46), p.1716-1722 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry 2019. ;Copyright Royal Society of Chemistry 2019 ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/c9sc03790j ;PMID: 32110351

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10
Catalyst-free depolymerization of polycaprolactone to silylated monoesters and iodide derivatives using iodosilanes
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Article
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Catalyst-free depolymerization of polycaprolactone to silylated monoesters and iodide derivatives using iodosilanes

Chemical communications (Cambridge, England), 2023-09, Vol.59 (75), p.11228-11231 [Peer Reviewed Journal]

Attribution - NonCommercial - NoDerivatives ;ISSN: 1359-7345 ;EISSN: 1364-548X ;DOI: 10.1039/D3CC03029f

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11
Intramolecular photochemical [2 + 1]-cycloadditions of nucleophilic siloxy carbenes
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Article
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Intramolecular photochemical [2 + 1]-cycloadditions of nucleophilic siloxy carbenes

Chemical science (Cambridge), 2022-03, Vol.13 (11), p.3273-3280 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2022 ;This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d2sc00203e ;PMID: 35414869

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12
Total synthesis of solanoeclepin A
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Article
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Total synthesis of solanoeclepin A

Nature chemistry, 2011-06, Vol.3 (6), p.484-488 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2011 ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/NCHEM.1044 ;PMID: 21602865

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13
The Hexane Extract of Citrus sphaerocarpa Ameliorates Visceral Adiposity by Regulating the PI3K/AKT/FoxO1 and AMPK/ACC Signaling Pathways in High-Fat-Diet-Induced Obese Mice
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Article
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The Hexane Extract of Citrus sphaerocarpa Ameliorates Visceral Adiposity by Regulating the PI3K/AKT/FoxO1 and AMPK/ACC Signaling Pathways in High-Fat-Diet-Induced Obese Mice

Molecules (Basel, Switzerland), 2023-12, Vol.28 (24), p.8026 [Peer Reviewed Journal]

2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules28248026 ;PMID: 38138517

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14
Asymmetric [4 + 2] cycloaddition synthesis of 4H-chromene derivatives facilitated by group-assisted-purification (GAP) chemistry
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Article
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Asymmetric [4 + 2] cycloaddition synthesis of 4H-chromene derivatives facilitated by group-assisted-purification (GAP) chemistry

RSC advances, 2021-12, Vol.11 (63), p.39790-39796 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2021 ;This journal is © The Royal Society of Chemistry 2021 The Royal Society of Chemistry ;EISSN: 2046-2069 ;DOI: 10.1039/d1ra08323f ;PMID: 35494146

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15
GC-MS Analysis and Biomedical Therapy of Oil from n-Hexane Fraction of Scutellaria edelbergii Rech . f.: In Vitro, In Vivo, and In Silico Approach
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Article
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GC-MS Analysis and Biomedical Therapy of Oil from n-Hexane Fraction of Scutellaria edelbergii Rech . f.: In Vitro, In Vivo, and In Silico Approach

Molecules (Basel, Switzerland), 2021-12, Vol.26 (24), p.7676 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules26247676 ;PMID: 34946757

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16
Photocyclization by a triplet-triplet annihilation upconversion pair in water - avoiding UV-light and oxygen removal
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Article
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Photocyclization by a triplet-triplet annihilation upconversion pair in water - avoiding UV-light and oxygen removal

Chemical science (Cambridge), 2023-10, Vol.14 (4), p.114-1144 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2023 ;This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d3sc03242f

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17
A benzothiazole-based new fluorogenic chemosensor for the detection of CN and its real-time application in environmental water samples and living cells
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Article
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A benzothiazole-based new fluorogenic chemosensor for the detection of CN and its real-time application in environmental water samples and living cells

RSC advances, 2022-03, Vol.12 (14), p.857-8577 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2022 ;This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d1ra08846g ;PMID: 35424806

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18
Base-promoted highly efficient synthesis of nitrile-substituted cyclopropanes via Michael-initiated ring closure
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Base-promoted highly efficient synthesis of nitrile-substituted cyclopropanes via Michael-initiated ring closure

RSC advances, 2022-10, Vol.12 (44), p.28576-28579 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2022 ;This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d2ra05393d

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19
Catalyzed ring transformation of cyclic N -aryl-azadiperoxides with participation of α,ω-dithiols
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Article
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Catalyzed ring transformation of cyclic N -aryl-azadiperoxides with participation of α,ω-dithiols

RSC advances, 2021-01, Vol.11 (7), p.4235-4236 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2021 ;This journal is © The Royal Society of Chemistry 2021 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d0ra09758f ;PMID: 35424327

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20
Investigating the efficacy of green solvents and solvent-free conditions in hydrogen-bonding mediated organocatalyzed model reactions
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Investigating the efficacy of green solvents and solvent-free conditions in hydrogen-bonding mediated organocatalyzed model reactions

RSC advances, 2024-03, Vol.14 (12), p.7992-7998 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2024 ;This journal is © The Royal Society of Chemistry 2024 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d4ra00679h ;PMID: 38454950

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