65212-13-7Relevant academic research and scientific papers
Expanded potential of seleno-carbohydrates as a molecular tool for X-ray structural determination of a carbohydrate-protein complex with single/multi-wavelength anomalous dispersion phasing
Suzuki, Tatsuya,Makyio, Hisayoshi,Ando, Hiromune,Komura, Naoko,Menjo, Masanori,Yamada, Yusuke,Imamura, Akihiro,Ishida, Hideharu,Wakatsuki, Soichi,Kato, Ryuichi,Kiso, Makoto
, p. 2090 - 2101 (2014/04/17)
Seleno-lactoses have been successfully synthesized as candidates for mimicking carbohydrate ligands for human galectin-9 N-terminal carbohydrate recognition domain (NCRD). Selenium was introduced into the mono- or di-saccharides using p-methylselenobenzoi
Selenium transfer reaction of primary selenoamides: A novel method for the synthesis of diacylselenides from acyl chlorides
Zhao, Hua-Rong,Zhao, Xin-Jian,Huang, Xian
, p. 3383 - 3387 (2007/10/03)
Diacyl selenides were afford in excent yields by reaction of primary selenoamides with acyl chlorides in chloroform. A possible mechanism is discussed.
Reactions of acyl chlorides with LiAlHSeH. Preparation of diacyl selenides, diacyl diselenides, selenocarboxylates and cyclic selenoanhydrides
Koketsu, Mamoru,Nada, Futoshi,Hiramatsu, Sohma,Ishihara, Hideharu
, p. 737 - 740 (2007/10/03)
Various diacyl selenides, diacyl diselenides and selenocarboxylates were synthesized by reaction of several acyl chlorides with LiAlHSeH. Reaction of diacyl chloride with LiAlHSeH afforded cyclic selenoanhydrides. In the 77Se NMR spectra, we fo
Reactions of O-Silyl Selenocarboxylates; IR and NMR Spectra of Heteroatom-substituted Selenocarboxylates
Kageyama, Hideki,Kido, Kenji,Kato, Shinzi,Murai, Toshiaki
, p. 1083 - 1088 (2007/10/02)
O-Silyl selenocarboxylates 1 react readily with acyl chlorides to give selenoanhydrides.Attempts to synthesize unsymmetrical selenoanhydrides selectively gave mixtures of the desired products with symmetrical selenoanhydrides.Ph3GeCl, Ph3SnCl, Ph3PbCl, Ph
