Potent DNA gyrase inhibitors bind asymmetrically to their target using symmetrical bifurcated halogen bonds
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Potent DNA gyrase inhibitors bind asymmetrically to their target using symmetrical bifurcated halogen bonds ; volume:12 ; number:1 ; day:8 ; month:1 ; year:2021 ; pages:1-13 ; date:12.2021
Nature Communications ; 12, Heft 1 (8.1.2021), 1-13, 12.2021
- Creator
-
Kolarič, Anja
Germe, Thomas
Hrast, Martina
Stevenson, Clare E. M.
Lawson, David M.
Burton, Nicolas P.
Vörös, Judit
Maxwell, Anthony
Minovski, Nikola
Anderluh, Marko
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-020-20405-8
- URN
-
urn:nbn:de:101:1-2021020600431253029358
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:27 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kolarič, Anja
- Germe, Thomas
- Hrast, Martina
- Stevenson, Clare E. M.
- Lawson, David M.
- Burton, Nicolas P.
- Vörös, Judit
- Maxwell, Anthony
- Minovski, Nikola
- Anderluh, Marko
- SpringerLink (Online service)
Other Objects (12)
N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
Activation of a metal-halogen bond by halogen bonding
Activation of a Metal‐Halogen Bond by Halogen Bonding †
Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
Lesson V. Symmetrical and skew symmetrical determinants.
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Fluoride Anions: Unexploited but Effective Halogen Bond Acceptors
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Photoexcited Transition‐Metal Catalyzed Carbon‐Halogen Bond Formation
N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
Activation of a metal-halogen bond by halogen bonding
Activation of a Metal‐Halogen Bond by Halogen Bonding †
Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
Lesson V. Symmetrical and skew symmetrical determinants.
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Fluoride Anions: Unexploited but Effective Halogen Bond Acceptors
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Photoexcited Transition‐Metal Catalyzed Carbon‐Halogen Bond Formation
N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
Activation of a metal-halogen bond by halogen bonding
Activation of a Metal‐Halogen Bond by Halogen Bonding †
Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
Lesson V. Symmetrical and skew symmetrical determinants.
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Fluoride Anions: Unexploited but Effective Halogen Bond Acceptors
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors