1970
DOI: 10.1039/c29700000978
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The orientation of free-radical addition to olefins

Abstract: S u m m a r y The rate and orientation of addition of hepta-olefins the substituent has virtually no effect on the rate of fluoropropyl radicals to a series of fluoro-olefins in the addition. Only with 1, l-difluoroethylene and 3,3,3-trigas phase has been determined by a competitive method. fluoropropene does there appear to be appreciable retarda-

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Cited by 6 publications
(2 citation statements)
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“…A more extended list (Table 8), taken from the work of Tedder and Walton and their colleagues, 36 illustrates this point more fully. A more extended list (Table 8), taken from the work of Tedder and Walton and their colleagues, 36 illustrates this point more fully.…”
Section: The Transition State In Radical Additionsmentioning
confidence: 93%
“…A more extended list (Table 8), taken from the work of Tedder and Walton and their colleagues, 36 illustrates this point more fully. A more extended list (Table 8), taken from the work of Tedder and Walton and their colleagues, 36 illustrates this point more fully.…”
Section: The Transition State In Radical Additionsmentioning
confidence: 93%
“…The deepcavity host 2 with a hydrophobic rim takes up gaseous butane in aqueous solution to form a 2:2 complex (Figure 1 b). [8] In this case, capsule formation is templated by guest encapsulation. Without the guest, only monomeric 2 is present in solution, as could be shown with DOSY NMR spectroscopy.…”
mentioning
confidence: 99%