51314-29-5Relevant articles and documents
Rhodium(III)-Catalyzed Synthesis of Naphthols via C-H Activation of Sulfoxonium Ylides
Xu, Youwei,Yang, Xifa,Zhou, Xukai,Kong, Lingheng,Li, Xingwei
, p. 4307 - 4310 (2017/08/23)
Direct and efficient synthesis of 1-naphthols has been realized via Rh(III)-catalyzed C-H activation of sulfoxonium ylides and subsequent annulation with alkynes, where the sulfoxonium ylide functioned as a new traceless bifunctional directing group. This reaction occurred under redox-neutral conditions with a broad substrate scope.
Studies on the tandem reaction of 4-aryl-2,3-allenoates with organozinc reagents: A facile route to polysubstituted naphthols
Chai, Guobi,Lu, Zhan,Fu, Chunling,Shengming, Ma.
supporting information; experimental part, p. 11083 - 11086 (2010/04/26)
A highly efficient tandem reaction of easily available 4-aryl-2,3- allenoates with organozinc reagents was developed to afford the diversified polysubstituted anaphthols in moderate to excellent yields. A solution of 4-bromophenyl zinc iodide and xylenes
Ring-expansion of 3-Arylinden-1-ones with Lithium Methylsulphinylmethanide
Buggle, Katherine,Ghogain, Una Ni,O'Sullivan, Daniel
, p. 2075 - 2076 (2007/10/02)
3,4-Disubstituted 1-naphthols (5a-h) are obtained in 49-89percent yield by the reaction of 2,3-disubstituted inden-1-ones (1a-h) with lithium methylsulphinylmethanide