118693-52-0Relevant academic research and scientific papers
Asymmetric Oxidative Cycloetherification of Naphtholic Alcohols
Jain, Nikita,Xu, Sanjia,Ciufolini, Marco A.
, p. 4542 - 4546 (2017/04/13)
The catalytic, enantioselective oxidative cyclization of naphthol-derived carboxylic acids mediated by chiral hypervalent iodine reagents has been studied extensively in the recent past, but analogous reactions of non-carboxylic substrates are yet unknown. This paper describes a catalytic, enantioselective, hypervalent iodine-promoted oxidative cycloetherification reaction of naphtholic alcohols. The new process relies on a variant of the Uyanik–Ishihara catalyst, in which the stereogenic centers have been relocated closer to the iodine atom. The new catalyst design affords optical yields comparable to those available with Uyanik–Ishihara iodides, but chemical yields are sensibly higher, at least with the tests substrates. An even more problematic reaction is the catalytic, enantioselective oxidative cyclization of naphtholic sulfonamides. In this case, the new catalyst affords significantly higher optical inductions than Uyanik–Ishihara iodides. The kinetic resolution of particular naphtholic alcohols is demonstrated. The absolute configuration of a numver of enantioenriched compounds obtained in this study was ascertained by X-ray diffractometry.
PHENOXIDE AND NAPHTHOXIDE IONS AS NUCLEOPHILES FOR SRN1 REACTIONS: SYNTHESIS OF BIPHENYL AND PHENYLNAPHTHYL DERIVATIVES
Beugelmans, Rene,Bois-Choussy, Michele
, p. 1289 - 1292 (2007/10/02)
Biphenyl or phenylnaphthyl derivatives are obtained by photostimulated SRN1 reactions between the anion of phenols or naphthols and variously substituted haloarenes.
