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Results 1 - 20 of 3,433,044  for All Library Resources

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1
Highly Efficient Base Catalyzed N-alkylation of Amines with Alcohols and β-Alkylation of Secondary Alcohols with Primary Alcohols
Highly Efficient Base Catalyzed N-alkylation of Amines with Alcohols and β-Alkylation of Secondary Alcohols with Primary Alcohols
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Highly Efficient Base Catalyzed N-alkylation of Amines with Alcohols and β-Alkylation of Secondary Alcohols with Primary Alcohols

ChemCatChem, 2023-10, Vol.15 (20) [Peer Reviewed Journal]

ISSN: 1867-3880 ;EISSN: 1867-3899 ;DOI: 10.1002/cctc.202300741

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2
Toxic Alcohols
Toxic Alcohols
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Toxic Alcohols

The New England journal of medicine, 2018-01, Vol.378 (3), p.270-280 [Peer Reviewed Journal]

Copyright © 2018 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMra1615295 ;PMID: 29342392

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3
Dehydrative Direct CH Allylation with Allylic Alcohols under [CpCoIII] Catalysis
Dehydrative Direct CH Allylation with Allylic Alcohols under [CpCoIII] Catalysis
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Dehydrative Direct CH Allylation with Allylic Alcohols under [CpCoIII] Catalysis

Angewandte Chemie (International ed.), 2015-08, Vol.54 (34), p.9944-9947 [Peer Reviewed Journal]

2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;Copyright Wiley Subscription Services, Inc. Aug 2015 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201503704 ;PMID: 26136375

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4
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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5
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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6
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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7
β‐Alkylation through Dehydrogenative Coupling of Primary Alcohols and Secondary Alcohols Catalyzed by Thioether‐Functionalized N‐Heterocyclic Carbene Ruthenium Complexes
β‐Alkylation through Dehydrogenative Coupling of Primary Alcohols and Secondary Alcohols Catalyzed by Thioether‐Functionalized N‐Heterocyclic Carbene Ruthenium Complexes
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β‐Alkylation through Dehydrogenative Coupling of Primary Alcohols and Secondary Alcohols Catalyzed by Thioether‐Functionalized N‐Heterocyclic Carbene Ruthenium Complexes

European journal of inorganic chemistry, 2023-08, Vol.26 (23) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1434-1948 ;EISSN: 1099-0682 ;DOI: 10.1002/ejic.202300188

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8
Tungsten-Catalyzed Regio- and Enantioselective Aminolysis of trans-2,3-Epoxy Alcohols: An Entry to Virtually Enantiopure Amino Alcohols
Tungsten-Catalyzed Regio- and Enantioselective Aminolysis of trans-2,3-Epoxy Alcohols: An Entry to Virtually Enantiopure Amino Alcohols
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Tungsten-Catalyzed Regio- and Enantioselective Aminolysis of trans-2,3-Epoxy Alcohols: An Entry to Virtually Enantiopure Amino Alcohols

Angewandte Chemie (International ed.), 2014-12, Vol.53 (50), p.13920-13923 [Peer Reviewed Journal]

2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;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.201408732 ;PMID: 25328028 ;CODEN: ACIEAY

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9
Tris(acetylacetonato)rhodium(III)-Catalyzed α-Alkylation of Ketones, β-Alkylation of Secondary Alcohols and Alkylation of Amines with Primary Alcohols
Tris(acetylacetonato)rhodium(III)-Catalyzed α-Alkylation of Ketones, β-Alkylation of Secondary Alcohols and Alkylation of Amines with Primary Alcohols
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Tris(acetylacetonato)rhodium(III)-Catalyzed α-Alkylation of Ketones, β-Alkylation of Secondary Alcohols and Alkylation of Amines with Primary Alcohols

Advanced synthesis & catalysis, 2013-06, Vol.355 (9), p.1859-1867 [Peer Reviewed Journal]

Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.201300061

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10
Iron-Catalyzed α-Alkylation of Ketones with Alcohols
Iron-Catalyzed α-Alkylation of Ketones with Alcohols
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Iron-Catalyzed α-Alkylation of Ketones with Alcohols

Angewandte Chemie (International ed.), 2015-11, Vol.54 (48), p.14483-14486 [Peer Reviewed Journal]

2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;Copyright Wiley Subscription Services, Inc. Nov 2015 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201506698 ;PMID: 26403489

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11
Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon
Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon
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Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon

Angewandte Chemie (International ed.), 2014-08, Vol.53 (35), p.9142-9150 [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.201403873 ;PMID: 25056771

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12
Efficient and Sustainable One-pot Synthesis of alpha-Carbonyl Homoallylic Alcohols from Benzaldehyde and Allylic Alcohols Using both NHC and Nickel Catalysts
Efficient and Sustainable One-pot Synthesis of alpha-Carbonyl Homoallylic Alcohols from Benzaldehyde and Allylic Alcohols Using both NHC and Nickel Catalysts
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Efficient and Sustainable One-pot Synthesis of alpha-Carbonyl Homoallylic Alcohols from Benzaldehyde and Allylic Alcohols Using both NHC and Nickel Catalysts

ChemCatChem, 2023-05, Vol.15 (10) [Peer Reviewed Journal]

Attribution ;ISSN: 1867-3899 ;EISSN: 1867-3899 ;DOI: 10.1002/cctc.202300038

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13
Yeast: the soul of beer’s aroma—a review of flavour-active esters and higher alcohols produced by the brewing yeast
Yeast: the soul of beer’s aroma—a review of flavour-active esters and higher alcohols produced by the brewing yeast
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Yeast: the soul of beer’s aroma—a review of flavour-active esters and higher alcohols produced by the brewing yeast

Applied microbiology and biotechnology, 2014-03, Vol.98 (5), p.1937-1949 [Peer Reviewed Journal]

Springer-Verlag Berlin Heidelberg 2014 ;COPYRIGHT 2014 Springer ;ISSN: 0175-7598 ;EISSN: 1432-0614 ;DOI: 10.1007/s00253-013-5470-0 ;PMID: 24384752

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14
Metallaphotoredox-enabled deoxygenative arylation of alcohols
Metallaphotoredox-enabled deoxygenative arylation of alcohols
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Metallaphotoredox-enabled deoxygenative arylation of alcohols

Nature (London), 2021-10, Vol.598 (7881), p.451-456 [Peer Reviewed Journal]

2021. The Author(s), under exclusive licence to Springer Nature Limited. ;COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Oct 21, 2021 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-021-03920-6 ;PMID: 34464959

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15
An Efficient and Recyclable Catalyst for N-Alkylation of Amines and β-Alkylation of Secondary Alcohols with Primary Alcohols: SBA-15 Supported N-Heterocyclic Carbene Iridium Complex
An Efficient and Recyclable Catalyst for N-Alkylation of Amines and β-Alkylation of Secondary Alcohols with Primary Alcohols: SBA-15 Supported N-Heterocyclic Carbene Iridium Complex
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An Efficient and Recyclable Catalyst for N-Alkylation of Amines and β-Alkylation of Secondary Alcohols with Primary Alcohols: SBA-15 Supported N-Heterocyclic Carbene Iridium Complex

Advanced synthesis & catalysis, 2013-04, Vol.355 (6), p.1117-1125 [Peer Reviewed Journal]

Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.201200732

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16
Direct Dehydroxytrifluoromethylthiolation of Alcohols Using Silver(I) Trifluoromethanethiolate and Tetra-n-butylammonium Iodide
Direct Dehydroxytrifluoromethylthiolation of Alcohols Using Silver(I) Trifluoromethanethiolate and Tetra-n-butylammonium Iodide
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Direct Dehydroxytrifluoromethylthiolation of Alcohols Using Silver(I) Trifluoromethanethiolate and Tetra-n-butylammonium Iodide

Angewandte Chemie (International ed.), 2015-01, Vol.54 (3), p.897-900 [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.201409983 ;PMID: 25420412 ;CODEN: ACIEAY

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17
Kinetic Resolution of 1,1′-Biaryl-2,2′-Diols and Amino Alcohols through NHC-Catalyzed Atroposelective Acylation
Kinetic Resolution of 1,1′-Biaryl-2,2′-Diols and Amino Alcohols through NHC-Catalyzed Atroposelective Acylation
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Kinetic Resolution of 1,1′-Biaryl-2,2′-Diols and Amino Alcohols through NHC-Catalyzed Atroposelective Acylation

Angewandte Chemie (International ed.), 2014-10, Vol.53 (41), p.11041-11045 [Peer Reviewed Journal]

2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;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.201406192 ;PMID: 25145856 ;CODEN: ACIEAY

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18
Enantioselective radical C-H amination for the synthesis of β-amino alcohols
Enantioselective radical C-H amination for the synthesis of β-amino alcohols
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Enantioselective radical C-H amination for the synthesis of β-amino alcohols

Nature chemistry, 2020-08, Vol.12 (8), p.697-704 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Nature Limited 2020. ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/s41557-020-0482-8 ;PMID: 32572164

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19
Cobalt-Catalyzed Alkylation of Aromatic Amines by Alcohols
Cobalt-Catalyzed Alkylation of Aromatic Amines by Alcohols
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Cobalt-Catalyzed Alkylation of Aromatic Amines by Alcohols

Angewandte Chemie (International ed.), 2015-12, Vol.54 (50), p.15046-15050 [Peer Reviewed Journal]

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.201507955 ;PMID: 26474443 ;CODEN: ACIEAY

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20
Visible light-induced direct α C-H functionalization of alcohols
Visible light-induced direct α C-H functionalization of alcohols
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Visible light-induced direct α C-H functionalization of alcohols

Nature communications, 2019-01, Vol.10 (1), p.467-7, Article 467 [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) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-08413-9 ;PMID: 30692540

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