A Chemical Approach to Introduce 2,6-Diaminopurine and 2-Aminoadenine Conjugates into Oligonucleotides without Need for Protecting Groups-Reference-Cited by-同舟云学术

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A Chemical Approach to Introduce 2,6-Diaminopurine and 2-Aminoadenine Conjugates into Oligonucleotides without Need for Protecting Groups

Published:2022-08-16 Issue:33 Volume:24 Page:6111-6116
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Madaoui Mimouna¹,Datta Dhrubajyoti¹,Wassarman Kelly¹,Zlatev Ivan¹,Egli Martin²^ORCID,Ross Bruce S.³,Manoharan Muthiah¹^ORCID

Affiliation:

1. Alnylam Pharmaceuticals, 675 West Kendall Street, Cambridge, Massachusetts 02142, United States

2. Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, Tennessee 37232, United States

3. Ross Chemistry Consulting, El Granada, California 94018, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c01848

Reference61 articles.

1. 2-Aminoadenine is an adenine substituting for a base in S-2L cyanophage DNA

2. Crystal Structure of A Z-DNA Fragment Containing Thymine/2-Aminoadenine Base Pairs

3. The influence of the purine 2-amino group on DNA conformation and stability-II

4. The influence of the purine 2-amino group on DNA conformation and stability. Synthesis and conformational analysis of d[T(2-aminoA)]3

5. The 2,6-Diaminopurine Riboside.cntdot.5-Methylisocytidine Wobble Base Pair: An Isoenergetic Substitution for the Study of G.cntdot.U Pairs in RNA

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