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Click Chemistry Inspired Synthesis of Hydroxyanthracene Triazolyl Glycoconjugates.

ABSTRACT: Novel hydroxyanthracene-based terminal alkynes 3 and 5a/b were synthesized by the acetylide addition reaction at the 9,10-position of anthraquinone 1 under mild conditions. The developed alkynes 3, 5a, and 5b on Huisgen azide-alkyne cycloaddition reaction with azido-sugars 6 in the presence of Cu(I) catalyst provided a series of triazole fasten hydroxyanthracene glycoconjugates 7, 8, and 9, respectively, in good yields. The representative compounds 9 and 7h were successfully deprotected under room-temperature conditions to liberate the corresponding free glycoconjugates 10 and 11, respectively. Further, structures of a few compounds were unmaliciously evidenced by their single-crystal X-ray.

SUBMITTER: Pandey N

PROVIDER: S-EPMC9608419 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

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Click Chemistry Inspired Synthesis of Hydroxyanthracene Triazolyl Glycoconjugates.

Pandey Nishant N Dwivedi Pratibha P Jyoti Singh Mangat M Kumar Dhananjay D Tiwari Vinod K VK Mishra Bhuwan B BB

ACS omega 20221013 42

Novel hydroxyanthracene-based terminal alkynes 3 and 5a/b were synthesized by the acetylide addition reaction at the 9,10-position of anthraquinone 1 under mild conditions. The developed alkynes 3, 5a, and 5b on Huisgen azide-alkyne cycloaddition reaction with azido-sugars 6 in the presence of Cu(I) catalyst provided a series of triazole fasten hydroxyanthracene glycoconjugates 7, 8, and 9, respectively, in good yields. ...[more]

PMID: 36312433

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