71098-98-1Relevant academic research and scientific papers
Radical intermediates in the Zn-promoted Barbier-type alkylation of diphenyl diselenide in aqueous medium
Dos Anjos, Jose Ayron Lira,Bieber, Lothar Wilhelm
, p. 6492 - 6494,3 (2012/12/12)
The zinc promoted Barbier-type reaction of alkyl halides and diphenyl diselenide in aqueous medium leads to high yields of mixed selenides even in acidic medium. Especially the efficient formation of t-butylphenylselenide cannot be explained by nucleophil
Cyclization of alkene-containing tetraalkylstannes
Herndon, James W.,Harp, Jill J.
, p. 6243 - 6246 (2007/10/02)
We have discovered a novel cyclization reaction, achieved through selective electrophilic cleavage of an organotin compound containing remote alkene functionality. The reaction has proven to be quite general with respect to a variety of substitution patte
N-PHENYLSELENOPHTHALIMIDE (NPSP) A VALUABLE SELENENYLATING AGENT
Nicolaou, K. C.,Petasis, N. A.,Claremon, D. A.
, p. 4835 - 4842 (2007/10/02)
The phenylseleno group (PhSe) has evolved in recent years as a very useful and versatile functionality.Its facile introduction into organic molecules and its subsequent oxidative or reductive removal, has allowed many important synthetic transformations.D
