An enantioselective and modular platform for C4'-modified nucleoside analogue synthesis enabled by intramolecular trans-acetalizations.
Saved in:
| Title: | An enantioselective and modular platform for C4'-modified nucleoside analogue synthesis enabled by intramolecular trans-acetalizations. |
|---|---|
| Authors: | Nuligonda T; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Kumar G; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Wang JW; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Rajapaksha D; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Elayan IA; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Demir R; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Meanwell NJ; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Wang SF; Department of Mathematics & Science, North Island College, Courtenay, BC, Canada., Mahal LK; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Brown A; Department of Chemistry, University of Alberta, Edmonton, AB, Canada., Meanwell MW; Department of Chemistry, University of Alberta, Edmonton, AB, Canada. meanwell@ualberta.ca. |
| Source: | Nature communications [Nat Commun] 2024 Aug 17; Vol. 15 (1), pp. 7080. Date of Electronic Publication: 2024 Aug 17. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
Be the first to leave a comment!
