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Articles by Dunyan Su
Isonitrile induced bioorthogonal activation of fluorophores and mutually orthogonal cleavage in live cells
Isonitrile induced bioorthogonal activation of fluorophores and mutually orthogonal cleavage in live cells† Xiaoyang Zhang, a Hui Xu,b Jie Li,b Dunyan Su,b Wuyu Mao,b Guohua Shen,a Lin Lia and Haoxing Wu *b Author affiliations * Corresponding authors a Laboratory of Clinical Nuclear Medicine, Department of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu 610041, China b Huaxi MR Research Center, Department of Radiology, Functional and Molecular Imaging Key Laboratory of...
Isonitrile induced bioorthogonal activation of fluorophores and mutually orthogonal cleavage in live cells
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68Ga‐prostate‐specific membrane antigen tracers can alter the management of more than half of prostate cancer patients with biochemical recurrence
COCHRANE REVIEW Zhiyun Jia Corresponding Author E-mail address: zhiyunjia@hotmail.com https://orcid.org/0000-0003-1886-5654 Department of Nuclear Medicine, West China Hospital of Sichuan University, Chengdu, PR China Corresponding Author Dr. Zhiyun Jia is to be contacted at Department of Nuclear Medicine, West China Hospital, Sichuan University, No. 37 Guo Xue Xiang, Chengdu, Sichuan (610041), PR China E‐mail: zhiyunjia@hotmail.com (Z.
Organocatalytic and Scalable Syntheses of Unsymmetrical 1,2,4,5‐Tetrazines by Thiol‐Containing Promotors
The full text of this article hosted at iucr.org is unavailable due to technical difficulties. Communication Organocatalytic and Scalable Syntheses of Unsymmetrical 1,2,4,5‐Tetrazines by Thiol‐Containing Promotors Prof.
Organocatalytic and Scalable Syntheses of Unsymmetrical 1,2,4,5‐Tetrazines by Thiol‐containing Promotors
Despite the growing application of tetrazine bioorthogonal chemistry, it is still challenging to access tetrazines conveniently from easily available materials. Here we describe de novo formation of tetrazine from nitriles and hydrazine hydrate using a broad array of thiol‐containing catalysts, including peptides. Using this facile methodology, we describe 14 syntheses of unsymmetric tetrazines containing a range of reactive functional groups on the gram scale with satisfactory yield.
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