Chiral helicenoid diarylethene with large change in specific optical rotation by photochromism1, 2

…, Y Tani, K Miyake, Y Yokoyama

Index: Okuyama, Tomoyuki; Tani, Yutaka; Miyake, Kentaro; Yokoyama, Yasushi Journal of Organic Chemistry, 2007 , vol. 72, # 5 p. 1634 - 1638

Full Text: HTML

Citation Number: 71

Abstract

A diarylethene possessing one [4] thiaheterohelicene and one benzothiophene, the latter with a chiral methoxymethoxyethyl group on its C-3 position, was proved to work as a switch of specific optical rotation at a wavelength at which both colored and colorless forms have no absorption in solution. The difference of the specific optical rotation was 1300° between the open form and the photostationary state. The specific optical rotation of one of the ...

Related Articles:

Lipase-catalyzed kinetic resolution of racemic 1-heteroarylethanols—experimental and QM/MM study

[Tosa, Monica; Pilbak, Sarolta; Moldovan, Paula; Paizs, Csaba; Szatzker, Gabor; Szakacs, Gyoergy; Novak, Lajos; Irimie, Florin-Dan; Poppe, Laszlo Tetrahedron Asymmetry, 2008 , vol. 19, # 15 p. 1844 - 1852]

High pressure and thermal Diels–Alder reaction of 2-vinyl-benzo [b] furan and 2-vinyl-benzo [b] thiophene. Synthesis of new condensed heterocycles

[Marrocchi, Assunta; Minuti, Lucio; Taticchi, Aldo; Scheeren, Hans W Tetrahedron, 2001 , vol. 57, # 23 p. 4959 - 4965]

More Articles...