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

^*この論文の責任著者

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

42 被引用数 (Scopus)

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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.

本文言語	英語
ページ（範囲）	10242-10244
ページ数	3
ジャーナル	Chemical Communications
巻	49
号	87
DOI	https://doi.org/10.1039/c3cc46055j
出版ステータス	出版済み - 2013/10/08

ASJC Scopus 主題領域

電子材料、光学材料、および磁性材料
触媒
セラミックおよび複合材料
化学一般
表面、皮膜および薄膜
金属および合金
材料化学

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10.1039/c3cc46055j

引用スタイル

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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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journal = "Chemical Communications",

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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

C2 - 24064857

AN - SCOPUS:84885415250

SN - 1359-7345

VL - 49

SP - 10242

EP - 10244

JO - Chemical Communications

JF - Chemical Communications

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ER -

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

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ASJC Scopus 主題領域

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