1,8-Naphthalimides as Stereochemical Probes for Chiral Amines: A Study of Electronic Transitions and Exciton Coupling-Reference-Cited by-同舟云学术

1,8-Naphthalimides as Stereochemical Probes for Chiral Amines: A Study of Electronic Transitions and Exciton Coupling

Published:1998-12-17 Issue:1 Volume:64 Page:234-241
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gawroński J.¹,Gawrońska K.¹,Skowronek P.¹,Holmén A.¹

Affiliation:

1. Department of Chemistry, A. Mickiewicz University, 60-780 Poznań, Poland, and Department of Physical Chemistry, Chalmers University of Technology, S-412 96 Gothenburg, Sweden

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo981760j

Reference31 articles.

1. Kaźmierczak, F.; Gawrońska, K.; Rychlewska, U.; Gawroński J.Tetrahedron: Asymmetry1994,5, 527.

2. Exciton coupling in various substituted aryl-phthalimide bichromophoric systems

3. Photoactivatable DNA-Cleaving Amino Acids: Highly Sequence-Selective DNA Photocleavage by Novel L-Lysine Derivatives

4. Photoinduced DNA Cleavage via Electron Transfer: Demonstration That Guanine Residues Located 5' to Guanine Are the Most Electron-Donating Sites

5. Theoretical Studies of GG-Specific Photocleavage of DNA via Electron Transfer: Significant Lowering of Ionization Potential and 5‘-Localization of HOMO of Stacked GG Bases in B-Form DNA

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