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Corrigendum: Expanding the Scope of PNA‐Encoded Synthesis (PES): Mtt‐Protected PNA Fully Orthogonal to Fmoc Chemistry and a Broad Array of Robust Diversity‐Generating Reactions
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The primers used contain chiral PNA residues that hybridize exclusively to d-DNA.
“However, the primers that were used contain chiral PNA residues22,41 that hybridize exclusively to d-DNA.42,43”
From Sequencing of d/l-DNA and XNA by Templated-Synthesis (2025) · cites this paper as [41]
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Cited by 2
Metadata
- Authors
- Chouikhi, D., Ciobanu, M., Zambaldo, C., Duplan, V., Barluenga, S., & Winssinger, N.
- ORCID
- Winssinger, Nicolas
- Venue
- Chemistry – A European Journal
- Publisher
- Wiley
- Published
- 2013-06-10
- Volume
- 19
- Issue
- 25
- Pages
- 8022-8022
- ISSN
- 0947-6539 (ISSN-L)
- 1521-3765
- OpenAlex
- W4229586889
- Cited by
- 2
- References
- 0
- Citations by year
- 2025: 1 · 2023: 1
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Chemistry - A European Journal (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Keywords
- peptide nucleic acid, Fmoc chemistry, orthogonal protecting groups, oligonucleotide synthesis
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