1,3-Dibromo-5,5-dimethylhydantoin as promoter for glycosylations using thioglycosides

Fei-Fei Xu, Claney L. Pereira and Peter H. Seeberger

Beilstein J. Org. Chem. 2017, 13, 1994–1998. https://doi.org/10.3762/bjoc.13.195

Supporting Information

Supporting Information File 1: Experimental details and full characterization data of all new compounds.
Format: PDF Size: 10.5 MB Download

References

Article Citation
Download RIS (Reference Manager) Download BIB (BIBTEX)
Cited References
Download RIS (Reference Manager) Download BIB (BIBTEX)

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.

Format: PNG Size: 105.8 KB Download
Back To Article

Latest Articles

Synthesis of meso-pyrrole-substituted corroles by condensation of 1,9-diformyldipyrromethanes with pyrrole

  1. Baris Temelli and
  2. Pinar Kapci
  • Full Research Paper
  • Published 06 Oct 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1403–1409, doi:10.3762/bjoc.18.145

Characterization of a new fusicoccane-type diterpene synthase and an associated P450 enzyme

  1. Jia-Hua Huang,
  2. Jian-Ming Lv,
  3. Liang-Yan Xiao,
  4. Qian Xu,
  5. Fu-Long Lin,
  6. Gao-Qian Wang,
  7. Guo-Dong Chen,
  8. Sheng-Ying Qin,
  9. Dan Hu and
  10. Hao Gao
  • Full Research Paper
  • Published 05 Oct 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1396–1402, doi:10.3762/bjoc.18.144

Preparation of an advanced intermediate for the synthesis of leustroducsins and phoslactomycins by heterocycloaddition

  1. Anaïs Rousseau,
  2. Guillaume Vincent and
  3. Cyrille Kouklovsky
  • Full Research Paper
  • Published 04 Oct 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1385–1395, doi:10.3762/bjoc.18.143

Synthesis of C6-modified mannose 1-phosphates and evaluation of derived sugar nucleotides against GDP-mannose dehydrogenase

  1. Sanaz Ahmadipour,
  2. Alice J. C. Wahart,
  3. Jonathan P. Dolan,
  4. Laura Beswick,
  5. Chris S. Hawes,
  6. Robert A. Field and
  7. Gavin J. Miller
  • Letter
  • Published 30 Sep 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1379–1384, doi:10.3762/bjoc.18.142

On drug discovery against infectious diseases and academic medicinal chemistry contributions

  1. Yves L. Janin
  • Perspective
  • Published 29 Sep 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1355–1378, doi:10.3762/bjoc.18.141

Cyclodextrin-based Schiff base pro-fragrances: Synthesis and release studies

  1. Attila Palágyi,
  2. Jindřich Jindřich,
  3. Juraj Dian and
  4. Sophie Fourmentin
  • Full Research Paper
  • Published 28 Sep 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1346–1354, doi:10.3762/bjoc.18.140

Synthesis and electrochemical properties of 3,4,5-tris(chlorophenyl)-1,2-diphosphaferrocenes

  1. Almaz A. Zagidullin,
  2. Farida F. Akhmatkhanova,
  3. Mikhail N. Khrizanforov,
  4. Robert R. Fayzullin,
  5. Tatiana P. Gerasimova,
  6. Ilya A. Bezkishko and
  7. Vasili A. Miluykov
  • Full Research Paper
  • Published 27 Sep 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1338–1345, doi:10.3762/bjoc.18.139

B–N/B–H Transborylation: borane-catalysed nitrile hydroboration

  1. Filip Meger,
  2. Alexander C. W. Kwok,
  3. Franziska Gilch,
  4. Dominic R. Willcox,
  5. Alex J. Hendy,
  6. Kieran Nicholson,
  7. Andrew D. Bage,
  8. Thomas Langer,
  9. Thomas A. Hunt and
  10. Stephen P. Thomas
  • Letter
  • Published 26 Sep 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1332–1337, doi:10.3762/bjoc.18.138

Computational model predicts protein binding sites of a luminescent ligand equipped with guanidiniocarbonyl-pyrrole groups

  1. Neda Rafieiolhosseini,
  2. Matthias Killa,
  3. Thorben Neumann,
  4. Niklas Tötsch,
  5. Jean-Noël Grad,
  6. Alexander Höing,
  7. Thies Dirksmeyer,
  8. Jochen Niemeyer,
  9. Christian Ottmann,
  10. Shirley K. Knauer,
  11. Michael Giese,
  12. Jens Voskuhl and
  13. Daniel Hoffmann
  • Full Research Paper
  • Published 23 Sep 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1322–1331, doi:10.3762/bjoc.18.137

Ionic multiresonant thermally activated delayed fluorescence emitters for light emitting electrochemical cells

  1. Merve Karaman,
  2. Abhishek Kumar Gupta,
  3. Subeesh Madayanad Suresh,
  4. Tomas Matulaitis,
  5. Lorenzo Mardegan,
  6. Daniel Tordera,
  7. Henk J. Bolink,
  8. Sen Wu,
  9. Stuart Warriner,
  10. Ifor D. Samuel and
  11. Eli Zysman-Colman
  • Full Research Paper
  • Published 22 Sep 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1311–1321, doi:10.3762/bjoc.18.136

Latest Articles

Latest Thematic Issues

Enzymes in biosynthesis

Jeroen S. Dickschat

New Show Issue

Molecular and macromolecular electrochemistry: synthesis, mechanism, and redox properties

Shinsuke Inagi and Mahito Atobe

New Show Issue

Mechanochemistry III

José G. Hernández and Lars Borchardt

New Show Issue

Platform and enabling technologies in organic synthesis

Philipp Heretsch and
Andreas Kirschning

2021 Show Issue

Organic TADF materials design

Eli Zysman-Colman

New Call Show Issue

Earth-abundant 3d metal catalysis

Lutz Ackermann

2021 Show Issue

Supramolecular approaches to mediate chemical reactivity

Carmine Gaeta, Pablo Ballester
and Qi-Qiang Wang

2021 Show Issue

New advances in asymmetric organocatalysis

Radovan Šebesta

2020 Show Issue

GlycoBioinformatics

Kiyoko F. Aoki-Kinoshita,
Frédérique Lisacek, Niclas Karlsson, 
Daniel Kolarich and Nicolle Packer

2020 Show Issue
Browse all Thematic Issues

Other Beilstein-Institut Open Science Activities

Logo
Logo
Logo
Logo

Keep Informed

RSS Feed

Subscribe to our Latest Articles RSS Feed.

Subscribe

Follow the Beilstein-Institut

LinkedIn

Twitter: @BeilsteinInst