A compatibility study on the glycosylation of 4, 4′-dihydroxyazobenzene. Issue 30 (5th May 2020)

• Record Type: Journal Article
• Authors: Berry, Jonathan; Despras, Guillaume; Lindhorst, Thisbe K.
• Is Part Of: RSC advances. Volume 10:Issue 30(2020)
• Page Start: 17432
• Page End: 17437
• Publication Date: 2020-05-05
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0ra02435j
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : The glycosylation of 4, 4′-dihydroxyazobenzene was investigated to identify suitable conditions providing access to valuable photoswitchable glycoconjugates. Abstract : Photoresponsive glycoconjugates based on the azobenzene photoswitch are valuable molecules which can be used as tools for the investigation of carbohydrate–protein interactions or as precursors of shape-switchable molecular architectures, for example. To access such compounds, glycosylation of 4, 4′-dihydroxyazobenzene (DHAB) is a critical step, frequently giving heterogeneous results because DHAB is a challenging glycosyl acceptor. Therefore, DHAB glucosylation was studied using nine different glycosyl donors, and reaction conditions were systematically varied in order to find a reliable procedure, especially towards the preparation of azobenzene bis-glucosides. Particular emphasis was put on glucosyl donors which were differentiated at the primary 6-position (N3, OAc) for further functionalisation. The present study allowed us to identify suitable glycosyl donors and reaction conditions matching with DHAB, affording the bis-glycosylated products in fair yields and good stereocontrol.