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Three different consecutive orbital symmetry-controlled reactions in the novel stereospecific synthesis of 1-phenyl-4-(1-phenylethenyl)naphthalene. The reaction of 3,4-diphenylthiophene 1,1-dioxide with ethynylbenzene

✍ Scribed by Nelb, R. G.; Stille, J. K.


Book ID
111678450
Publisher
American Chemical Society
Year
1976
Tongue
English
Weight
785 KB
Volume
98
Category
Article
ISSN
0002-7863

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## Abstract Reactions of electron‐poor α‐haloketones with (__N__‐isocyanimino) triphenylphosphorane in the presence of aromatic carboxylic acids proceed smoothly at room temperature and in neutral conditions to afford disubstituted 1,3,4‐oxadiazole derivatives in high yields. © 2010 Wiley Periodica