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Results 1 - 20 of 778,002  for All Library Resources

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1
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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2
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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3
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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4
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 Edition, 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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5
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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6
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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7
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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8
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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9
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. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201408732 ;PMID: 25328028

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10
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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11
Alcohols as alkylating agents in heteroarene C-H functionalization
Alcohols as alkylating agents in heteroarene C-H functionalization
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Alcohols as alkylating agents in heteroarene C-H functionalization

Nature (London), 2015-09, Vol.525 (7567), p.87-90 [Peer Reviewed Journal]

COPYRIGHT 2015 Nature Publishing Group ;COPYRIGHT 2015 Nature Publishing Group ;Copyright Nature Publishing Group Sep 3, 2015 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature14885 ;PMID: 26308895 ;CODEN: NATUAS

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12
Copper-catalysed enantioselective stereodivergent synthesis of amino alcohols
Copper-catalysed enantioselective stereodivergent synthesis of amino alcohols
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Copper-catalysed enantioselective stereodivergent synthesis of amino alcohols

Nature (London), 2016-04, Vol.532 (7599), p.353-356 [Peer Reviewed Journal]

COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group Apr 21, 2016 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature17191 ;PMID: 27018656 ;CODEN: NATUAS

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13
Rh-Catalyzed CC Cleavage of Benzyl/Allylic Alcohols to Produce Benzyl/Allylic Amines or other Alcohols by Nucleophilic Addition of Intermediate Rhodacycles to Aldehydes and Imines
Rh-Catalyzed CC Cleavage of Benzyl/Allylic Alcohols to Produce Benzyl/Allylic Amines or other Alcohols by Nucleophilic Addition of Intermediate Rhodacycles to Aldehydes and Imines
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Rh-Catalyzed CC Cleavage of Benzyl/Allylic Alcohols to Produce Benzyl/Allylic Amines or other Alcohols by Nucleophilic Addition of Intermediate Rhodacycles to Aldehydes and Imines

Chemistry : a European journal, 2012-12, Vol.18 (50), p.16214-16225 [Peer Reviewed Journal]

Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.201201867 ;PMID: 23080063

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14
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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15
syn-1,2-Amino Alcohols via Diastereoselective Allylic C−H Amination
syn-1,2-Amino Alcohols via Diastereoselective Allylic C−H Amination
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syn-1,2-Amino Alcohols via Diastereoselective Allylic C−H Amination

Journal of the American Chemical Society, 2007-06, Vol.129 (23), p.7274-7276 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja071905g ;PMID: 17516648

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16
A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular CO Bond Formation with Secondary and Primary Alcohols
A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular CO Bond Formation with Secondary and Primary Alcohols
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A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular CO Bond Formation with Secondary and Primary Alcohols

Angewandte Chemie (International ed.), 2011-10, Vol.50 (42), p.9943-9947 [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.201104361 ;PMID: 21913292

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17
Copper-Catalyzed Tandem Trifluoromethylation/Semipinacol Rearrangement of Allylic Alcohols
Copper-Catalyzed Tandem Trifluoromethylation/Semipinacol Rearrangement of Allylic Alcohols
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Copper-Catalyzed Tandem Trifluoromethylation/Semipinacol Rearrangement of Allylic Alcohols

Angewandte Chemie (International ed.), 2013-09, Vol.52 (37), p.9781-9785 [Peer Reviewed Journal]

Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201304557 ;PMID: 23868806 ;CODEN: ACIEAY

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18
Hydrogenation of Esters to Alcohols with a Well-Defined Iron Complex
Hydrogenation of Esters to Alcohols with a Well-Defined Iron Complex
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Hydrogenation of Esters to Alcohols with a Well-Defined Iron Complex

Angewandte Chemie (International ed.), 2014-08, Vol.53 (33), p.8722-8726 [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.201402542 ;PMID: 24890043 ;CODEN: ACIEAY

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19
2-Azaadamantane N-Oxyl (AZADO) and 1-Me-AZADO:  Highly Efficient Organocatalysts for Oxidation of Alcohols
2-Azaadamantane N-Oxyl (AZADO) and 1-Me-AZADO:  Highly Efficient Organocatalysts for Oxidation of Alcohols
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2-Azaadamantane N-Oxyl (AZADO) and 1-Me-AZADO:  Highly Efficient Organocatalysts for Oxidation of Alcohols

Journal of the American Chemical Society, 2006-07, Vol.128 (26), p.8412-8413 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja0620336 ;PMID: 16802802 ;CODEN: JACSAT

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20
Compartmentalization of metabolic pathways in yeast mitochondria improves the production of branched-chain alcohols
Compartmentalization of metabolic pathways in yeast mitochondria improves the production of branched-chain alcohols
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Compartmentalization of metabolic pathways in yeast mitochondria improves the production of branched-chain alcohols

Nature biotechnology, 2013-04, Vol.31 (4), p.335-341 [Peer Reviewed Journal]

COPYRIGHT 2013 Nature Publishing Group ;COPYRIGHT 2013 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2013 ;ISSN: 1087-0156 ;EISSN: 1546-1696 ;DOI: 10.1038/nbt.2509 ;PMID: 23417095

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