Self‐Assembly and Biorecognition of a Spirohydantoin Derived from α‐Tetralone: Interplay between Chirality and Intermolecular Interactions-Reference-Cited by-同舟云学术

Self‐Assembly and Biorecognition of a Spirohydantoin Derived from α‐Tetralone: Interplay between Chirality and Intermolecular Interactions

Published:2020-06 Issue:6 Volume:85 Page:1220-1232
ISSN:2192-6506
Container-title:ChemPlusChem
language:en
Short-container-title:ChemPlusChem

Author:

Lazić Anita M.¹^ORCID,Đorđević Ivana S.²,Radovanović Lidija D.¹,Popović Dragan M.²,Rogan Jelena R.³,Janjić Goran V.²,Trišović Nemanja P.³

Affiliation:

1. Innovation Centre of the Faculty of Technology and Metallurgy Karnegijeva 4 11120 Belgrade Serbia

2. Department of Chemistry – Theoretical chemistry and molecular modelingInstitute of Chemistry, Technology and MetallurgyNational InstituteUniversity of Belgrade Njegoševa 12 11000 Belgrade Serbia

3. Department of General and Inorganic ChemistryDepartment of Organic ChemistryFaculty of Technology and MetallurgyUniversity of Belgrade Karnegijeva 4, 11120 Belgrade (Serbia)

Funder

Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cplu.202000273

Reference41 articles.

1. Are Racemic Crystals Favored over Homochiral Crystals by Higher Stability or by Kinetics? Insights from Comparative Studies of Crystalline Stereoisomers

2. Enantioselective recognition of an isomeric ligand by a biomolecule: mechanistic insights into static and dynamic enantiomeric behavior and structural flexibility

3. Bridging Crystal Engineering and Drug Discovery by Utilizing Intermolecular Interactions and Molecular Shapes in Crystals

4. Recent applications of hydantoin and thiohydantoin in medicinal chemistry

5. Privileged Scaffolds or Promiscuous Binders: A Comparative Study on Rhodanines and Related Heterocycles in Medicinal Chemistry

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