79296-92-7Relevant articles and documents
Br?nsted acid-catalysed conjugate addition of photochemically generated α-amino radicals to alkenylpyridines
Hepburn, Hamish B.,Melchiorre, Paolo
supporting information, p. 3520 - 3523 (2016/03/04)
The conjugate addition of α-amino radicals to alkenylpyridines has been accomplished by the synergistic merger of Br?nsted acid and visible light photoredox catalysis. Key to reaction development was the protonation of the alkenylpyridines that transientl
Phthalazine derivatives for treating inflammatory diseases
-
, (2008/06/13)
The invention relates to the treatment of an inflammatory disease, especially an inflammatory rheumatoid or rheumatic disease, and/or pain with an inhibitor of the activity of VEGF receptor tyrosine kinase of the formula I, wherein r is 0 to 2, n is 0 to
SYNTHESIS OF CAROTENOID ANALOGUES HAVING PYRIDINE, FURAN, AND TIOPHENE RINGS AS TERMINAL GROUPS
Brahmana, Hemat R.,Katsuyama, Kazuki,Inanaga, Junji,Katsuki, Tsutomi,Yamaguchi, Masaru
, p. 1695 - 1696 (2007/10/02)
Heteroaromatic carotenoid analogues having 2-pyridyl, 3-pyridyl, 2-furyl, 3-furyl, 2-thienyl, and 3-thienyl groups at both the ends of tetramethyloctadecanonaene chain, were synthesized and their spectral properties were examined.