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Volumn 38, Issue 1-2, 1999, Pages 219-222

Amidation of [Rh(I)(ethene)]+ via a 2-rhodaoxetane

Author keywords

Alkene complexes; Amidations; C N coupling; Oxidations; Rhodium

Indexed keywords

ALKENE; RHODIUM DERIVATIVE;

EID: 0033556067     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1521-3773(19990115)38:1/2<219::aid-anie219>3.0.co;2-i     Document Type: Article
Times cited : (28)

References (49)
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    • The few isolated 2-metallaoxetanes known are all stabilized by various substituents. Consequently, it is difficult to deduce the intrinsic reactivity of the unsubstituted 2-metallaoxetane moiety from these substituted examples: a) V. W. Day, W. G. Klemperer, S. P. Lockledge, D. J. Main, J Am. Chem. Soc. 1990, 112, 2031;
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    • note
    • Details of the crystal structure determination are available as supporting information on the WWW.
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    • note
    • 2O.
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    • 2+. see D. L. Thorn, J. C. Calabrese, J. Organomet. Chem. 1984, 272, 283. For other examples of nitrile C≡N-bond activation by metal coordination (including Pinner type reactions with alcohols), see B. N. Storhoff, H. C. Lewis Jr., Coord. Chem. Rev. 1977, 23, 1
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    • 2+. see D. L. Thorn, J. C. Calabrese, J. Organomet. Chem. 1984, 272, 283. For other examples of nitrile C≡N-bond activation by metal coordination (including Pinner type reactions with alcohols), see B. N. Storhoff, H. C. Lewis Jr., Coord. Chem. Rev. 1977, 23, 1
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    • Storhoff, B.N.1    Lewis H.C., Jr.2
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    • Wiley, and references therein
    • For the Pinner syntheses, see J. March, Advanced Organic Chemistry, 4th ed, Wiley, 1992, p. 892, and references therein. For the Ritter reaction, see J. March, Advanced Organic Chemistry, 4th ed, Wiley, 1992, p. 970. and references therein.
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    • For the Pinner syntheses, see J. March, Advanced Organic Chemistry, 4th ed, Wiley, 1992, p. 892, and references therein. For the Ritter reaction, see J. March, Advanced Organic Chemistry, 4th ed, Wiley, 1992, p. 970. and references therein.
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    • note
    • 2 · MeOH, respectively. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ. UK (fax: (+44) 1223-336-033: e-mail: deposit@ccdc.cam.ac.uk)
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    • The thermal decomposition of alkylalkanimidates yields, among others, nitriles and alcohols or trisubstituted 1.3.5-triazines and alcohols: a) F. Cramer, K. Pawelzik, J. Kupper, Angew. Chem. 1956, 20, 649;
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    • Cramer, F.1    Pawelzik, K.2    Kupper, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.