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Use of isotopic labeling in establishing reaction mechanisms: CD+3 + C2H6

✍ Scribed by Christian Berg; Wolfgang Wachter; Thomas Schindler; Christian Kronseder; Gereon Niedner-Schatteburg; Vladimir E. Bondybey; Zdenek Herman


Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
497 KB
Volume
216
Category
Article
ISSN
0009-2614

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✦ Synopsis


The reaction of CD: with C2H6 has been reinvestigated by the Fourier-transform ion cyclotron resonance technique. It proceeds, in addition to the previously observed "hydride transfer" pathway resulting in the C,H: ion, by at least two other channels. "Methylene transfer" results in the isotopic C2H2D: ion, and "eliminative condensation" accompanied by molecular hydrogen ejection results in several Cs ionic products. The reactions are investigated as a function of the collision energy, and their possible mechanisms are discussed.


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## Abstract A synthetic route to isotopically labelled forms of the tropane alkaloid hyoscyamine, including (__RS__)‐[3β€², 3β€²,‐^2^H~2~]‐ (**2a**) and (__RS__)‐[1′‐^13^C, 3β€², 3β€²,‐^2^H~2~]‐ (**2b**) hyoscyamines, involving the reaction between phenylacetyl tropine and formaldehyde is described. The is