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[1]
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Steering the Surface-Confined Self-Assembly of Multifunctional Star-Shaped Molecules
The Journal of Physical Chemistry C,
2023
DOI:10.1021/acs.jpcc.3c02638
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[2]
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Enantioselective C-C Bond Forming Reactions: From Metal Complex-, Organo-, and Bio-catalyzed Perspectives
Advances in Catalysis,
2023
DOI:10.1016/bs.acat.2023.10.001
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[3]
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Chirality determination in crystals
Chirality,
2022
DOI:10.1002/chir.23377
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[4]
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Chirality determination in crystals
Chirality,
2022
DOI:10.1002/chir.23377
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[5]
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The self‐disproportionation of enantiomers (SDE): The effect of scaling down, potential problems versus prospective applications, possible new occurrences, and unrealized opportunities?
ELECTROPHORESIS,
2019
DOI:10.1002/elps.201800414
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[6]
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Late-Stage Fluorination of Bioactive Molecules and Biologically-Relevant Substrates
2019
DOI:10.1016/B978-0-12-812958-6.00010-0
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[7]
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The self-disproportionation of enantiomers (SDE): The effect of scaling down, potential problems versus prospective applications, possible new occurrences, and unrealized opportunities?
ELECTROPHORESIS,
2019
DOI:10.1002/elps.201800414
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[8]
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The self-disproportionation of enantiomers (SDE) of amino acids and their derivatives
Amino Acids,
2019
DOI:10.1007/s00726-019-02729-y
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[9]
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The self-disproportionation of enantiomers (SDE): a menace or an opportunity?
Chemical Science,
2018
DOI:10.1039/C7SC05138G
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[10]
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A question of policy: should tests for the self-disproportionation of enantiomers (SDE) be mandatory for reports involving scalemates?
Tetrahedron: Asymmetry,
2017
DOI:10.1016/j.tetasy.2017.08.020
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[11]
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Remarkable magnitude of the self-disproportionation of enantiomers (SDE) via achiral chromatography: application to the practical-scale enantiopurification of β-amino acid esters
Amino Acids,
2016
DOI:10.1007/s00726-015-2152-5
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[12]
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Nonracemic γ-Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters
European Journal of Organic Chemistry,
2016
DOI:10.1002/ejoc.201600520
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[13]
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Nonracemic γ‐Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ‐Unsaturated Carboxylic Esters
European Journal of Organic Chemistry,
2016
DOI:10.1002/ejoc.201600520
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[14]
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Total Syntheses of (−)-Mersicarpine, (−)-Scholarisine G, (+)-Melodinine E, (−)-Leuconoxine, (−)-Leuconolam, (−)-Leuconodine A, (+)-Leuconodine F, and (−)-Leuconodine C: Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon for Scholarisine G and Leuconodines A and C
Journal of the American Chemical Society,
2015
DOI:10.1021/jacs.5b03619
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[15]
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Total Syntheses of (−)-Mersicarpine, (−)-Scholarisine G, (+)-Melodinine E, (−)-Leuconoxine, (−)-Leuconolam, (−)-Leuconodine A, (+)-Leuconodine F, and (−)-Leuconodine C: Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon for Scholarisine G and Leuconodines A and C
Journal of the American Chemical Society,
2015
DOI:10.1021/jacs.5b03619
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[16]
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Terminology Related to the Phenomenon ‘Self-Disproportionation of Enantiomers’ (SDE)
Helvetica Chimica Acta,
2014
DOI:10.1002/hlca.201400122
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[17]
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Terminology Related to the Phenomenon ‘Self‐Disproportionation of Enantiomers’ (SDE)
Helvetica Chimica Acta,
2014
DOI:10.1002/hlca.201400122
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