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  Photo-labile BODIPY protecting groups for glycan synthesis

Leichnitz, S., Dissanayake, K. C., Winter, A. H., & Seeberger, P. H. (2022). Photo-labile BODIPY protecting groups for glycan synthesis. Chemical Communications, 58(75), 10556-10559. doi:10.1039/D2CC03851J.

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Leichnitz, Sabrina1, Author           
Dissanayake, Komadhie C., Author
Winter, Arthur H., Author
Seeberger, Peter H.1, Author           
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1Peter H. Seeberger - Vaccine Development, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863308              

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 Abstract: Protective groups that can be selectively removed under mild conditions are an essential aspect of carbohydrate chemistry. Groups that can be selectively removed by visible light are particularly attractive because carbohydrates are transparent to visible light. Here, different BODIPY protecting groups were explored for their utility during glycan synthesis. A BODIPY group bearing a boron difluoride unit is stable during glycosylations but can be cleaved with green light as illustrated by the assembly of a trisaccharide.

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Language(s): eng - English
 Dates: 2022-09-012022
 Publication Status: Published in print
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 Identifiers: DOI: 10.1039/D2CC03851J
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Title: Chemical Communications
  Abbreviation : Chem. Commun.
Source Genre: Journal
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Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: - Volume / Issue: 58 (75) Sequence Number: - Start / End Page: 10556 - 10559 Identifier: ISSN: 1359-7345