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Volumn 47, Issue 38, 2006, Pages 6831-6834

Nucleophile-solvent isotope effects between methanol isotopomers during the interception of aziridinium imide-'like' closed intermediates

Author keywords

Ene reactions; Solvent addition; Solvent isotope effects; Triazolinediones

Indexed keywords

2 METHYL 2 BUTENE; 2,3 DIMETHYL 2 BUTENE; ALKENE DERIVATIVE; AZIRIDINE DERIVATIVE; ISOBUTYLENE; ISOTOPE; METHANOL; METHYL GROUP; N PHENYLTRIAZOLINEDIONE; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33747198040     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.07.063     Document Type: Article
Times cited : (8)

References (58)
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    • (1980) Reaction Rates of Isotopic Molecules
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    • Buncel E., and Lee C.C. (Eds), Elsevier
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    • (1987) Secondary and Solvent Isotope Effects , vol.7 , pp. 1-60
    • Schowen, R.L.1    Alvarez, F.J.2
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    • Buncel E., and Lee C.C. (Eds), Elsevier
    • Kresge A.J., More O'Ferrall R.A., and Powell M.F. In: Buncel E., and Lee C.C. (Eds). Solvent Isotope Effects, Fractionation Factors and Mechanisms of proton Transfer Reactions; Isotopes in Organic Chemistry. Secondary and Solvent Isotope Effects Vol. 7 (1987), Elsevier 177-273
    • (1987) Secondary and Solvent Isotope Effects , vol.7 , pp. 177-273
    • Kresge, A.J.1    More O'Ferrall, R.A.2    Powell, M.F.3
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    • 2).
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    • 3OH).
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    • note
    • In such a case we could have uneven competition between the two nucleophile-solvents because of: (i) a possible primary isotope effect during -H(D) transfer, and (ii) a secondary isotope effect during the nucleophilic addition through hyperconjugation, both of which would have favored the -OH bearing solvent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.