87880-38-4Relevant academic research and scientific papers
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)
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.
An Efficient Synthesis of Naphthalenic Lignan Lactones
Gokhale, S. M.,Joshi, R. R.,Narasimhan, N. S.
, p. 1030 - 1034 (2007/10/02)
Phthalides (1a-c) have been converted into the corresponding naphthalenic diesters (3a-c) and anhydrides (11, 15) through silyloxyisobenzofurans (2a-c), generated in situ, by reaction with respective dienophiles.The naphthalenic lignan lactones (4a-c), in
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
