A novel application of the Staudinger ligation to access neutral cyclic di-nucleotide analog precursors via a divergent method
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Journal articleDate
2017-06-07Department
ChemistryPermanent link to this record
http://hdl.handle.net/20.500.12613/8385
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https://doi.org/10.1039/c7ra06045aAbstract
Our efforts to develop a scalable and divergent synthesis of cyclic di-nucleotide analog precursors have resulted in (1) an orthogonally protected di-amino carbohydrate as well as (2) the novel application of the Staudinger ligation to provide medium-sized macrocycles featuring carbamate or urea linkages.Citation
RSC Adv., 2017,7, 29835-29838Citation to related work
Royal Society of ChemistryHas part
RSC Advances, Iss. 47ADA compliance
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http://dx.doi.org/10.34944/dspace/8352