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Lee, Choi Chuck, Ko, Eric C. F. (1978) Rearrangement studies with 14C. XLII. The solvolysis of triphenylvinyl-2-14C bromide in aqueous acetic acid and in 2,2,2-trifluoroethanol. Canadian Journal of Chemistry, 56 (18). 2459-2466 doi:10.1139/v78-402

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Reference TypeJournal (article/letter/editorial)
TitleRearrangement studies with 14C. XLII. The solvolysis of triphenylvinyl-2-14C bromide in aqueous acetic acid and in 2,2,2-trifluoroethanol
JournalCanadian Journal of Chemistry
AuthorsLee, Choi ChuckAuthor
Ko, Eric C. F.Author
Year1978 (September 15)Volume56
Issue18
PublisherCanadian Science Publishing
DOIdoi:10.1139/v78-402Search in ResearchGate
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Mindat Ref. ID8304969Long-form Identifiermindat:1:5:8304969:9
GUID0
Full ReferenceLee, Choi Chuck, Ko, Eric C. F. (1978) Rearrangement studies with 14C. XLII. The solvolysis of triphenylvinyl-2-14C bromide in aqueous acetic acid and in 2,2,2-trifluoroethanol. Canadian Journal of Chemistry, 56 (18). 2459-2466 doi:10.1139/v78-402
Plain TextLee, Choi Chuck, Ko, Eric C. F. (1978) Rearrangement studies with 14C. XLII. The solvolysis of triphenylvinyl-2-14C bromide in aqueous acetic acid and in 2,2,2-trifluoroethanol. Canadian Journal of Chemistry, 56 (18). 2459-2466 doi:10.1139/v78-402
In(1978, September) Canadian Journal of Chemistry Vol. 56 (18) Canadian Science Publishing

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Lee, Choi Chuck, Ko, Eric C. F. (1976) Rearrangement studies with 14C. XLI. Degenerate rearrangements in vinyl cations from triphenylvinyl-2-14C-phenyltriazene and from trianisylvinyl-2-14C-phenyltriazene. Canadian Journal of Chemistry, 54 (19). 3041-3044 doi:10.1139/v76-431
Lee, Choi Chuck, Ko, Eric C. F., Rappoport, Zvi (1980) Rearrangement studies with 14C. XLIV. Ion-pairs and dissociated ions in the solvolysis of triphenyl[2-14C]vinyl and trianisyl[2-14C]vinyl bromides in 70% acetic acid – 30% water. Canadian Journal of Chemistry, 58 (22). 2369-2376 doi:10.1139/v80-381
Lee, Choi Chuck, Obafemi, Craig A. (1981) Rearrangement studies with 14C. XLV. The decomposition of cis- and trans-1,2-dianisyl-2-phenyl[2-14C]vinylphenyltriazenes in acetic acid. Canadian Journal of Chemistry, 59 (11). 1636-1640 doi:10.1139/v81-242
Lee, Choi Chuck, Cessna, Allan J., Davis, Bruce A., Oka, Mitsuo (1974) Rearrangement Studies with 14C. XXXIX. 1,2-Phenyl Shifts in Solvolyses of Triphenylvinyl-2-14C Triflate. Canadian Journal of Chemistry, 52 (15). 2679-2683 doi:10.1139/v74-390
Lee, C. C., Unger, D., Vassie, Sharon (1972) Rearrangement Studies with 14C. XXXVI. Solvolysis of 1-14C-2-Phenylethyl Tosylate in Aqueous Acetic Acid with or without Added Sodium Azide. Canadian Journal of Chemistry, 50 (9). 1371-1375 doi:10.1139/v72-214
Lee, Choi Chuck, Weber, Ursula, Obafemi, Craig A. (1979) Rearrangement studies with 14C. XLIII. The acetolysis of trianisyl[2-14C]vinyl bromide. Canadian Journal of Chemistry, 57 (11). 1384-1387 doi:10.1139/v79-225
Rummens, Franz H. A., Green, Robert D., Cessna, Allan J., Oka, Mitsuo, Lee, Choi Chuck (1975) 13C Nuclear Magnetic Resonance and 14C Tracer Studies on 1,2-Phenyl Shifts in the Reaction of Labeled Triphenylvinyl Bromide with Acetic Acid and Silver Acetate. Canadian Journal of Chemistry, 53 (3). 314-319 doi:10.1139/v75-044
Lee, Choi Chuck, Reichle, Randy, Weber, Ursula (1978) Protonated cyclopropanes. X. Studies on the deamination of n-butylamine-1-14C and the decomposition of 3-(n-butyl-1-14C)-1-phenyltriazene. Canadian Journal of Chemistry, 56 (5). 658-662 doi:10.1139/v78-108
Lee, Choi Chuck, Unger, Don (1974) Rearrangement Studies with 14C. XL. The Acetolysis of 2-Phenylethyl-1-14C Triflate. Canadian Journal of Chemistry, 52 (23). 3955-3959 doi:10.1139/v74-591
Lee, Choi Chuck, Obafemi, Craig A., Quail, J. Wilson, Rappoport, Zvi (1981) Rearrangement studies with 14C. XLVI. Isotopic scrambling studies on the acetolysis of trianisylvinyl bromide labeled with 13C and with 14C. Canadian Journal of Chemistry, 59 (15). 2342-2349 doi:10.1139/v81-338
Lee, Choi Chuck, Wanigasekera, Dave, Fiakpui, Charles Y. (1986) Solvolyses of some 13C- or 14C-labeled triarylvinyl bromides in aqueous acetic acid. Canadian Journal of Chemistry, 64 (6). 1235-1239 doi:10.1139/v86-205
 
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