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- Se–N interactions in selenohydroxylamine: a theoretical study. Prasad V. Bharatam, Rajnish Moudgil, Damanjit Kaur
, J. Chem. Soc., Perkin Trans. 2
, 2000
, 2469
- N-(Diphenylphosphinothioyl)hydroxylamine: preparation, characterisation and base-induced transposition of sulfur and oxygen atoms in its O-benzoyl derivative 1. Martin J. P. Harger
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 3205
- Genetic incorporation of 1,2-aminothiol functionality for site-specific protein modification via thiazolidine formation. Xiaobao Bi, Kalyan Kumar Pasunooti, Ahmad Hussen Tareq, John Takyi-Williams, Chuan-Fa Liu
, Org. Biomol. Chem.
, 2016
, 14
, 5282
- Real time monitoring of aminothiol level in blood using a near-infrared dye assisted deep tissue fluorescence and photoacoustic bimodal imaging. Palapuravan Anees, James Joseph, Sivaramapanicker Sreejith, Nishanth Venugopal Menon, Yuejun Kang, Sidney Wing-Kwong Yu, Ayyappanpillai Ajayaghosh, Yanli Zhao
, Chem. Sci.
, 2016
, 7
, 4110
- Quinones as novel chemiluminescent probes for the sensitive and selective determination of biothiols in biological fluids. Mohamed Saleh Elgawish, Naoya Kishikawa, Naotaka Kuroda
, Analyst
, 2015
, 140
, 8148
- Accelerated reduction and solubilization of elemental sulfur by 1,2-aminothiols. Jonathan T. Stoffel, Kimberly T. Riordan, Emily Y. Tsui
, Chem. Commun.
, 2021
, 57
, 12488
- A novel clickable MSAP agent for dual fluorescence/nuclear labeling of biovectors. Kuo-Ting Chen, Jim Nieuwenhuizen, Maryana Handula, Yann Seimbille
, Org. Biomol. Chem.
, 2020
, 18
, 6134
- Direct synthesis of N-sulfenylimines through oxidative coupling of amines with disulfides/thiols over copper based metal–organic frameworks. Wei Long, Wenge Qiu, Chuanqiang Li, Liyun Song, Guangmei Bai, Guizhen Zhang, Hong He
, RSC Adv.
, 2016
, 6
, 40945
- A unique reaction of diphenylcyclopropenone and 1,2-aminothiol with the release of thiol for multiple bioconjugation. Shanshan Liu, Haishun Ye, Long Yi, Zhen Xi
, Chem. Commun.
, 2023
, 59
, 1497
- Catalyst-free thiazolidine formation chemistry enables the facile construction of peptide/protein–cell conjugates (PCCs) at physiological pH. Xiangquan Liu, Youyu Wang, Bangce Ye, Xiaobao Bi
, Chem. Sci.
, 2023
, 14
, 7334