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pro vyhledávání: '"Tunng-Hsien Lee"'
Autor:
Tunng-Hsien Lee, 李東憲
99
This thesis studies on photorearrangement of 3-styrylfurans to synthesize 2-methylnaphthalenes in basic media. A series of reactants, 3-styrylfurans, was synthesized by Wittig or Wittig-Horner reactions. Irradiation of these reactants in meth
This thesis studies on photorearrangement of 3-styrylfurans to synthesize 2-methylnaphthalenes in basic media. A series of reactants, 3-styrylfurans, was synthesized by Wittig or Wittig-Horner reactions. Irradiation of these reactants in meth
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/hpqd3h
Publikováno v:
Tetrahedron. 70:1748-1762
The construction of different types of substituted arenes was demonstrated through the photocyclization of 2-(fur-3-yl)ethenylarenes using a 3-furyl group as an isopropenyl equivalent synthon in the photocyclization reaction. The furan portion of the
Publikováno v:
Tetrahedron Letters. 52:7199-7201
Irradiation of 3-(4-substituted styryl)furans in basic media yielded a series of 7-substituted-2-methylnaphthalenes, including methoxy, isopropyl, ethyl, methyl, fluoro, and cyano substituents. This base-induced photorearrangement involves cis–tran
Publikováno v:
ChemInform. 45
The construction of different types of substituted arenes was demonstrated through the photocyclization of 2-(fur-3-yl)ethenylarenes using a 3-furyl group as an isopropenyl equivalent synthon in the photocyclization reaction. The furan portion of the
Publikováno v:
ChemInform. 43
Irradiation of 3-(4-substituted styryl)furans in basic media yielded a series of 7-substituted-2-methylnaphthalenes, including methoxy, isopropyl, ethyl, methyl, fluoro, and cyano substituents. This base-induced photorearrangement involves cis–tran