Coupling reaction of thioamides with sulfonyl azides: An efficient catalyst-free click-type ligation under mild conditions

Muhammad Aswad; Junya Chiba; Takenori Tomohiro; Yasumaru Hatanaka

doi:10.1039/c3cc46055j

Coupling reaction of thioamides with sulfonyl azides: An efficient catalyst-free click-type ligation under mild conditions

Muhammad Aswad, Junya Chiba^*, Takenori Tomohiro, Yasumaru Hatanaka

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

42 Scopus citations

Abstract

We report a coupling reaction of thioamides and sulfonyl azides to generate sulfonyl amidines in the absence of any activation additives. The reaction progresses in various solvents under mild conditions. Water exhibits the highest performance with respect to efficiency.

Original language	English
Pages (from-to)	10242-10244
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	87
DOIs	https://doi.org/10.1039/c3cc46055j
State	Published - 2013/10/08

ASJC Scopus subject areas

Electronic, Optical and Magnetic Materials
Catalysis
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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title = "Coupling reaction of thioamides with sulfonyl azides: An efficient catalyst-free click-type ligation under mild conditions",

abstract = "We report a coupling reaction of thioamides and sulfonyl azides to generate sulfonyl amidines in the absence of any activation additives. The reaction progresses in various solvents under mild conditions. Water exhibits the highest performance with respect to efficiency.",

author = "Muhammad Aswad and Junya Chiba and Takenori Tomohiro and Yasumaru Hatanaka",

year = "2013",

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doi = "10.1039/c3cc46055j",

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AU - Aswad, Muhammad

AU - Chiba, Junya

AU - Tomohiro, Takenori

AU - Hatanaka, Yasumaru

PY - 2013/10/8

Y1 - 2013/10/8

N2 - We report a coupling reaction of thioamides and sulfonyl azides to generate sulfonyl amidines in the absence of any activation additives. The reaction progresses in various solvents under mild conditions. Water exhibits the highest performance with respect to efficiency.

AB - We report a coupling reaction of thioamides and sulfonyl azides to generate sulfonyl amidines in the absence of any activation additives. The reaction progresses in various solvents under mild conditions. Water exhibits the highest performance with respect to efficiency.

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U2 - 10.1039/c3cc46055j

DO - 10.1039/c3cc46055j

M3 - 学術論文

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JO - Chemical Communications

JF - Chemical Communications

IS - 87

ER -

Coupling reaction of thioamides with sulfonyl azides: An efficient catalyst-free click-type ligation under mild conditions

Abstract

ASJC Scopus subject areas

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