Mild and Efficient Functionalization at C6 of Purine 2‘-Deoxynucleosides and Ribonucleosides1
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602-5700
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol000255h
Reference20 articles.
1. Palladium-Catalyzed C−N Bond Formation: Facile and General Synthesis of N6-Aryl 2‘-Deoxyadenosine Analogues
2. Facile Synthesis of O6-Alkyl-, O6-Aryl-, and Diaminopurine Nucleosides from 2‘-Deoxyguanosine
3. Postsynthetic Generation of a Major Acrolein Adduct of 2‘-Deoxyguanosine in Oligomeric DNA†
4. A General Method for the Synthesis of the N2- and N6- Carcinogenic Amine Adducts of 2‘-Deoxyguanosine and 2‘-Deoxyadenosine1
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