C–H functionalization of triazolo[a]-annulated 8-azapurines-Reference-Cited by-同舟云学术

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C–H functionalization of triazolo[a]-annulated 8-azapurines

Published:2016-05 Issue:21 Volume:57 Page:2303-2305
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Gorbunov Evgeny B.,Rusinov Gennady L.,Ulomsky Evgeny N.,Rusinov Vladimir L.,Charushin Valery N.,Chupakhin Oleg N.

Funder

Russian Foundation for Basic Research

Russian Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. Heterocyclic Chemistry in Drug Discovery;Jack Li,2013

2. Molecules and Medicine;Corey,2008

3. Synthesis and biological evaluation of novel homochiral carbocyclic nucleosides from 1-amino-2-indanols

4. SYNTHESIS, ANTIVIRAL AND CYTOSTATIC ACTIVITIES, OF CARBOCYCLIC NUCLEOSIDES INCORPORATING A MODIFIED CYCLOPENTANE RING. IV. ADENOSINE AND URIDINE ANALOGUES

5. Acyclic Nucleotide Analogs Derived from 8-Azapurines: Synthesis and Antiviral Activity

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1. Metal free C(sp2) H functionalization of nitrogen heterocycles;Advances in Heterocyclic Chemistry;2024

2. Pyrazolo[1,5-a]pyrimidine with similar “amino–nitro–amino” arrangement characteristics to TATB: a novel heat-resistant explosive with fused structure;CrystEngComm;2021

3. Direct synthetic routes to functionalised crown ethers;Organic Chemistry Frontiers;2021

4. Synthesis of Pyrimidine-Annulated Five-Membered Heterocycles: An Overview;Current Organic Chemistry;2019-12-24

5. Nucleophilic C—H functionalization of arenes: a contribution to green chemistry;Russian Chemical Bulletin;2019-03

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