64241-58-3Relevant articles and documents
Discovery of Fluorogenic Diarylsydnone-Alkene Photoligation: Conversion of ortho-Dual-Twisted Diarylsydnones into Planar Pyrazolines
Zhang, Linmeng,Zhang, Xiaocui,Yao, Zhuojun,Jiang, Shichao,Deng, Jiajie,Li, Bo,Yu, Zhipeng
supporting information, p. 7390 - 7394 (2018/06/13)
A small library of diarylsydnones (DASyds) was constructed based on aryl-pairing combinations and subjected to click reaction toward alkenes under photoirradiation with high efficiency. We were able to demonstrate the utility of DASyds for highly fluorescent turn-on ligation targeting the trans-cyclooct-4-en-1-ol moieties on protein.
Activated carbonyl species for the preparation of ortho-acylarylsydnones
Turnbull, Kenneth,Beladakere, Ravindra N.,McCall, Neal D.
, p. 383 - 388 (2007/10/03)
ortho-Acylarylsydnones can be prepared in moderate to good yield by the action of nucleophiles upon suitable activated carbonyl species.
DEBROMINATION OF 4-BROMO-3-ARYLSYDNONES WITH SODIUM SULFITE
McChord, K. L.,Tullis, S. A.,Turnbull, K.
, p. 2249 - 2253 (2007/10/02)
4-Bromo-3-arylsydnones 1 are debrominated to the corresponding 3-arylsydnones 2 in good to excellent yield using sodium sulfite in methanol/water.In contrast to previously employed reagents, the reaction is successful in the presence of electron-donating,
