Results 291 to 300 of about 153,572 (317)
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Cycloadditions to the Azulene System
Angewandte Chemie International Edition in English, 1970Cycloadditions to the azulene system have not hitherto been observed. Instead, azulene reacts, e.g., with maleic anhydride via an "addition-substitution route" to give 1-azulenylsuccinic anhydride and with tetracyanoethylene to yield 1-tricy-anovinylazulene[¹].
Hafner, Klaus, Häring, J., Jäkel, W.
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ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Takanori Matsuda, Masahiro Murakami
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AbstractFor Abstract see ChemInform Abstract in Full Text.
Takanori Matsuda, Masahiro Murakami
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ChemInform, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Angel Díaz-Ortiz +2 more
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AbstractFor Abstract see ChemInform Abstract in Full Text.
Angel Díaz-Ortiz +2 more
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Cycloadditions and Cycloreversions I. [2+2]-Cycloaddition
1992It was pointed out in the preceding chapter that correlation diagrams can be read from right to left as easily as from left to right. This is certainly true from the formal viewpoint of orbital symmetry, but does not preclude the need to examine the geometric and energetic consequences of the nuclear motions involved.
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Angewandte Chemie, 1970
Die Homofulvene (Ia) bzw. (Ib) lassen sich in einer K-carbonat-Losung mit N-Chlorsulfonylisocyanat bei -60°C in einer Homo-[6+2]-Cycloaddition unter Inversion an C-6 zu den Addukten (IIa) bzw. (IIb) umsetzen.
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Die Homofulvene (Ia) bzw. (Ib) lassen sich in einer K-carbonat-Losung mit N-Chlorsulfonylisocyanat bei -60°C in einer Homo-[6+2]-Cycloaddition unter Inversion an C-6 zu den Addukten (IIa) bzw. (IIb) umsetzen.
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Cycloadditions. VIII. Cycloaddition of vinyl azides to ketenes
The Journal of Organic Chemistry, 1972Makhluf J. Haddadin +2 more
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