A Study on the Intramolecular Mitsunobu Reaction of N 6 -(ω-Hydroxyalkyl)adenines-Reference-Cited by-同舟云学术

A Study on the Intramolecular Mitsunobu Reaction of N 6 -(ω-Hydroxyalkyl)adenines

Published:2017-09-08 Issue:6 Volume:54 Page:3565-3573
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J. Heterocyclic Chem.

Author:

Šimůnková Naděžda¹,Tobrman Tomáš¹,Eigner Václav²,Dvořák Dalimil¹^ORCID

Affiliation:

1. Department of Organic Chemistry; University of Chemistry and Technology, Prague; Technická 5 166 28 Prague 6 Czech Republic

2. Department of Solid State Chemistry; University of Chemistry and Technology, Prague; Technická 5 166 28 Prague 6 Czech Republic

Funder

Ministry of Education, Youth and Sports of the Czech Republic

Grantová Agentura České Republiky

Research Centre “The Structure and Synthetic Applications of Transition Metal Complexes−LC06070” of the Ministry of Education, Youth and Sports of the Czech Republic

Publisher

Wiley

Subject

Organic Chemistry

Reference30 articles.

1. Miscoding properties of 1,N6-ethanoadenine, a DNA adduct derived from reaction with the antitumor agent 1,3-bis(2-chloroethyl)-1-nitrosourea

2. Chloroethylnitrosourea-derived ethano cytosine and adenine adducts are substrates for Escherichia coli glycosylases excising analogous etheno adducts

3. Exocyclic Deoxyadenosine Adducts of 1,2,3,4-Diepoxybutane: Synthesis, Structural Elucidation, and Mechanistic Studies

4. Discovery of α-Aminoazaheterocycle-Methylglyoxal Adducts as a New Class of High-Affinity Inhibitors of Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels

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