910131-03-2Relevant academic research and scientific papers
Synthesis of chiral dotriacontanaphthalenes: How many naphthalene units are we able to elaborately connect?
Sue, Daisuke,Takaishi, Kazuto,Harada, Takunori,Kuroda, Reiko,Kawabata, Takeo,Tsubaki, Kazunori
supporting information; scheme or table, p. 3940 - 3943 (2009/11/30)
(Chemical Equation Presented) (S,S,S,S,S,S,S,S,S,S,S,S,S,S,S,S,S,S,S,S,S,S, S,S,S,S,S,S,S,S,S)-dotriacontanaphthalenes 32A-E alternately possessing butoxy and methoxy side chains were precisely constructed through a bottom-up synthesis, and their absolute
Bottom-up synthesis of optically active oligonaphthalenes: Three different pathways for controlling axial chirality
Tsubaki, Kazunori,Tanaka, Hiroyuki,Takaishi, Kazuto,Miura, Masaya,Morikawa, Hiroshi,Furuta, Takumi,Tanaka, Kiyoshi,Fuji, Kaoru,Sasamori, Takahiro,Tokitoh, Norihiro,Kawabata, Takeo
, p. 6579 - 6587 (2007/10/03)
The oxidative homocoupling of optically active binaphthalenes 1a-d with a stoichiometric amount of CuCl2 and amines afforded quaternaphthalenes 2a-d in up to 93% de. The high diastereoselectivities were achieved through three different pathways
