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Thiazolidine chemistry revisited : a fast, efficient and stable click-type reaction at physiological pH

Bermejo-Velasco, Daniel (author)
Uppsala universitet,Polymerkemi
Nawale, Ganesh N. (author)
Uppsala universitet,Polymerkemi
Oommen, Oommen P. (author)
Bioengineering and Nanomedicine Lab, Faculty of Biomedical Sciences and Engineering, Tampere University of Technology, and BioMediTech Institute, 33720, Tampere, Finland
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Hilborn, Jöns, 1956- (author)
Uppsala universitet,Polymerkemi
Varghese, Oommen P., 1977- (author)
Uppsala universitet,Polymerkemi
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 (creator_code:org_t)
2018
2018
English.
In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 54:88, s. 12507-12510
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We describe the fast reaction kinetics between 1,2-aminothiols and aldehydes. Under physiological conditions such a click-type reaction afforded a thiazolidine product that remains stable and did not require any catalyst. This type of bioorthogonal reaction offers enormous potential for the coupling of biomolecules in an efficient and biocompatible manner.

Subject headings

NATURVETENSKAP  -- Kemi -- Polymerkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Polymer Chemistry (hsv//eng)

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