1608-42-0Relevant articles and documents
Construction of new fluorophores by Diels-Alder reaction of diacenaphthothiophenes
Yamamoto, Yuma,Fukuoka, Yoshiaki,Nishida, Jun-ichi,Kitamura, Chitoshi,Kawase, Takeshi
, p. 5725 - 5730 (2017)
The Diels–Alder (DA) reaction of diacenaphtheno[1,2-b;1′,2′-d]thiophene (1a) with benzyne affords 1:1 and 1:2 adducts, 7 and 8, in 47 and 11% yields. An X-ray crystallographic analysis reveals that 8 possesses a dibenzobarrelene structure involving a rigi
THE ADDITION OF BENZYNE TO AZULENE
Cresp, Terry M.,Wege, Dieter
, p. 6713 - 6718 (1986)
The title reaction afforded the Diels-Alder adduct 4b,10-etheno-benzazulene (4), while an analogous reacton involving 5,6-dichloroazulene gave the 6,7- and 7,8-dichloro-derivatives of (4).Treatment of (4) with 3,6-di(pyridin-2-yl)-s-tetrazine yielded b
Application of deuterated THENA for assigning the absolute configuration of chiral secondary alcohols
Soponpong, Jakapun,Dolsophon, Kulvadee,Thongpanchang, Chawanee,Linden, Anthony,Thongpanchang, Tienthong
, p. 497 - 500 (2019)
The structure of a constrained bicyclic chiral derivatizing agent (CDA), 1,2,3,4-tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid, THENA 1, was modified by replacing both exo-methylene protons with deuterium atoms. The modified CDA, THENA-d2 2
NOVEL ANTHRACENE DERIVATIVES AND ORGANIC ELECTRONIC DEVICE USING SAME
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Page/Page column 32-33, (2011/06/23)
The present invention provides a novel anthracene derivatives and an organic electronic device using the same. Thte organic electronic device according to the present invention shows excellent properties in terms of efficiency, a driving voltage, and a life span.
