42407-05-6Relevant articles and documents
Silicon-rhodamine isothiocyanate for fluorescent labelling
Nasufovi?, Veselin,Then, Patrick,Dr?ge, Fabian,Duong, Michael,Kaether, Christoph,Dietzek, Benjamin,Heintzmann, Rainer,Arndt, Hans-Dieter
supporting information, p. 574 - 578 (2021/02/06)
An efficient synthesis for silicon-rhodamines was developed, enabling the preparation and evaluation of silicon-rhodamine isothiocyanate (SITC) as a novel tool for facile fluorescent labeling. Ease of use in conjugation to amino groups, high stability and excellent photophysical properties are demonstrated. SITC-actin was found to be neutral to F-actin polymerization induction and well suited for high resolution fluorescence microscopy.
Facile Syntheses of Oxazolines and Thiazolines with N-Acylbenzotriazoles under Microwave Irradiation
Katritzky, Alan R.,Cai, Chunming,Suzuki, Kazuyuki,Singh, Sandeep K.
, p. 811 - 814 (2007/10/03)
Microwave reactions of 2-amino-2-methyl-1-propanol (2) or 2-aminoethanethiol hydrochloride (4) with readily available N-acylbenzotriazoles 1a-j in the presence of SOCl2 produced 2-substituted 2-oxazolines 3a-j in 84-98% yields and 2-substituted
Natural Kaolinitic clay catalyzed conversion of nitriles to 2-oxazolines
Jnaneshwara,Deshpande,Lalithambika,Ravindranathan,Bedekar
, p. 459 - 462 (2007/10/03)
Natural Kaolinitic clay has been found effective as catalyst in the conversion of aromatic and aliphatic nilriles with 1,2-aminoalcohol to 2-oxazolines (56-96%, yield).