In-cell indirect electrochemical halogenation of pyrimidine bases and their nucleosides to 5-haloderivatives-Reference-Cited by-同舟云学术

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In-cell indirect electrochemical halogenation of pyrimidine bases and their nucleosides to 5-haloderivatives

Published:1992-12 Issue:50 Volume:33 Page:7779-7782
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Palmisano G.,Danieli B.,Santagostino M.,Vodopivec B.,Fiori G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. On the alleged electrochemical methoxylation of ergolines

2. Electrochemical Synthesis of 2-Haloergolines

3. Electrochemical heterocyclization of o-toluenesulfonamides to 3-alkyl-4,5-dihydro-1,2,4-benzothiazepine-1,1-dioxides

4. Selectivity in the thiocyanation of 3-alkylindoles: an unexpectedly easy access to 2-isothiocyano derivatives

5. Cerium(IV)-mediated halogenation at C-5 of uracil derivatives

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Halogenation of Carbonyl and Related Compounds;Comprehensive Organic Transformations;2018-02-28

2. ChemInform Abstract: In-Cell Indirect Electrochemical Halogenation of Pyrimidine Bases and Their Nucleosides to 5-Halo Derivatives.;ChemInform;2010-08-20

3. Indirect Electrochemical Reactions;Encyclopedia of Electrochemistry;2004-06-24

4. A mild and effective iodination method using iodine in the presence of bis-(trifluoroacetoxy)iodobenzene;Tetrahedron Letters;1998-09

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