Sulfur fluoride exchange-Reference-Cited by-同舟云学术

Sulfur fluoride exchange

Published:2023-08-03 Issue:1 Volume:3 Page:
ISSN:2662-8449
Container-title:Nature Reviews Methods Primers
language:en
Short-container-title:Nat Rev Methods Primers

Author:

Homer Joshua A.^ORCID,Xu Long,Kayambu Namitharan^ORCID,Zheng Qinheng^ORCID,Choi Eun Joung,Kim Byeong Moon^ORCID,Sharpless K. Barry^ORCID,Zuilhof Han^ORCID,Dong Jiajia^ORCID,Moses John E.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,General Biochemistry, Genetics and Molecular Biology

Link

https://www.nature.com/articles/s43586-023-00241-y.pdf

Reference150 articles.

1. Kolb, H. C., Finn, M. G. & Sharpless, K. B. Click chemistry: diverse chemical function from a few good reactions. Angew. Chem. Int. Ed. 40, 2004–2021 (2001). This is the original click chemistry manifesto presented by K. Barry Sharpless, outlining the synthesis philosophy and requirements for a reaction to achieve ‘click’ status.

2. Rostovtsev, V. V., Green, L. G., Fokin, V. V. & Sharpless, K. B. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective ‘ligation’ of azides and terminal alkynes. Angew. Chem. Int. Ed. 41, 2596–2599 (2002).

3. Tornøe, C. W., Christensen, C. & Meldal, M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J. Org. Chem. 67, 3057–3064 (2002).

4. Agard, N. J., Prescher, J. A. & Bertozzi, C. R. A strain-promoted [3 + 2] azide−alkyne cycloaddition for covalent modification of biomolecules in living systems. J. Am. Chem. Soc. 126, 15046–15047 (2004).

5. Dong, J., Krasnova, L., Finn, M. G. & Sharpless, K. B. Sulfur(VI) fluoride exchange (SuFEx): another good reaction for click chemistry. Angew. Chem. Int. Ed. 53, 9430–9448 (2014). This publication represents the re-emergence of SuFEx as a click reaction and describes in detail many of the unique properties of S–F-containing substrates.

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