John D. Jolliffe

ORCID: 0000-0003-3341-9572
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Axial and Atropisomeric Chirality Synthesis
  • Crystallography and molecular interactions
  • Molecular spectroscopy and chirality
  • Asymmetric Synthesis and Catalysis
  • Alkaloids: synthesis and pharmacology
  • Cyclopropane Reaction Mechanisms
  • Radical Photochemical Reactions
  • Research Data Management Practices
  • Photochromic and Fluorescence Chemistry
  • Synthetic Organic Chemistry Methods
  • Oxidative Organic Chemistry Reactions
  • Digital Humanities and Scholarship
  • Catalytic C–H Functionalization Methods
  • Academic Writing and Publishing
  • Asymmetric Hydrogenation and Catalysis
  • Mathematics, Computing, and Information Processing
  • Chemistry and Chemical Engineering
  • Scientific Computing and Data Management
  • Health and Medical Research Impacts
  • Ethics in Clinical Research
  • Surface Chemistry and Catalysis
  • Library Science and Information Systems
  • History and advancements in chemistry

Johannes Gutenberg University Mainz
2023

Newcastle University
2021

Oxford Research Group
2016-2019

University of Oxford
2016-2019

Technical University of Munich
2018

British Museum
1968

Abstract BINOLs are valuable and widely used building blocks, chiral ligands, catalysts that effective across a remarkable range of different chemical transformations. Here we demonstrate an ammonium salt catalyzed kinetic resolution racemic with benzyl tosylate proceeds s up to 46. This is scalable practical process can be applied >30 C 2 ‐ non‐ ‐symmetric BINOLs. Implementation this method enables the enantioselective synthesis wide BINOL derivatives over 99:1 e.r.

10.1002/anie.201814381 article EN cc-by Angewandte Chemie International Edition 2019-02-19

Abstract Das erste Gesetz der Photochemie, das auf Theodor von Grotthuß und John W. Draper zurückgeht, besagt, dass nur Teil des Lichts, durch Materie absorbiert wird, eine Wirkung hervorruft. Entsprechend lässt sich Reaktionsverhalten einer chemischen Verbindung steuern, wenn ihr Absorptionsverhalten Emission Lichtquelle angepasst wird. Eine chemische mit einem Chromophor, bei niedrigen Wellenlänge Licht absorbiert, wird langwellige Strahlung nicht angeregt. Gelingt es reversible...

10.1002/ange.201804006 article DE cc-by-nc Angewandte Chemie 2018-05-28

Abstract An approach to the intramolecular Diels–Alder reaction has led a cascade synthesis of complex carbocycles composed three fused rings and up five stereocenters with complete stereocontrol. Computational analysis reveals that proceeds by Michael/Michael/cyclopropanation/epimerization in which size coordination counterion is key.

10.1002/anie.201608534 article EN cc-by Angewandte Chemie International Edition 2016-10-07

Abstract BINOLs are valuable and widely used building blocks, chiral ligands, catalysts that effective across a remarkable range of different chemical transformations. Here we demonstrate an ammonium salt catalyzed kinetic resolution racemic with benzyl tosylate proceeds s up to 46. This is scalable practical process can be applied >30 C 2 ‐ non‐ ‐symmetric BINOLs. Implementation this method enables the enantioselective synthesis wide BINOL derivatives over 99:1 e.r.

10.1002/ange.201814381 article EN cc-by Angewandte Chemie 2019-02-19

The conversion of large files catalogue information requires, in addition to the manpower for keypunching, a considerable amount preediting by professional staff. An experiment machine editing and tagging unedited but structured demonstrated possibility eliminating effort from majority records.

10.1108/eb026451 article EN Journal of Documentation 1968-03-01

An approach to the intramolecular Diels–Alder reaction has led a cascade synthesis of complex carbocycles composed three fused rings and up five stereocenters with complete stereocontrol. Computational analysis reveals that proceeds by Michael/Michael/cyclopropanation/epimerization in which size coordination counterion is key.

10.1002/ange.201608534 article EN cc-by Angewandte Chemie 2016-10-07

Abstract The National Research Data Infrastructure for Chemistry (NFDI4Chem) has been providing a lot of useful resources and support chemists two years now.

10.1002/nadc.20224131398 article EN Nachrichten aus der Chemie 2022-09-01

In this manuscript, we examine the role of errors in data-driven research and assess extent to which issue has been addressed across various fields. It presents examples how scientific communities have related problems highlights observations on newly developed error cultures can positively impact process. We do against backdrop Germany’s effort facilitate data sharing through a National Research Data Infrastructure (NFDI) was initiated 2018. demonstrate, both benefit from suitable...

10.31219/osf.io/kruhn preprint EN 2024-09-13

In der Struktur des vorgeschlagenen Übergangszustands 47 in Abbildung 1 dieser Zuschrift ist Katalysator falsch gezeichnet. Eine korrigierte Fassung daher hier gezeigt. Proposed mechanism of observed kinetic resolution. Die Autoren bitten um Entschuldigung für diesen Fehler, keinerlei Auswirkungen auf die Schlussfolgerungen hat.

10.1002/ange.201904626 article DE Angewandte Chemie 2019-05-20
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