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Volumn 53, Issue 51, 2014, Pages 14175-14180

Ruthenium-porphyrin-catalyzed diastereoselective intramolecular alkyl carbene insertion into C-H bonds of alkyl diazomethanes generated in situ from N-tosylhydrazones

Author keywords

Alkyl carbenes; Alkyl diazomethanes; C H insertion; Homogeneous catalysis; Ruthenium

Indexed keywords

CARBONYL COMPOUNDS; CATALYSIS; CATALYST SELECTIVITY; PORPHYRINS; REACTION KINETICS; RUTHENIUM; SYNTHESIS (CHEMICAL);

EID: 84917674412     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201408102     Document Type: Article
Times cited : (85)

References (49)
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    • For the use of alkyl diazomethanes in scandium(III)-catalyzed intermolecular carbon insertion into formyl C-H bonds through ScIII activation of aldehyde substrates, see: A. J. Wommack, D. C. Moebius, A. L. Travis, J. S. Kingsbury, Org. Lett. 2009, 11, 3202;
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    • Wommack, A.J.1    Moebius, D.C.2    Travis, A.L.3    Kingsbury, J.S.4
  • 11
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    • for stoichiometric C-H insertion of iron, niobium, or tantalum alkyl carbene species, see: a) S. Ishii, S. Zhao, P. Helquist, J. Am. Chem. Soc. 2000, 122, 5897;
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 5897
    • Ishii, S.1    Zhao, S.2    Helquist, P.3
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    • Angew. Chem. 2011, 123, 7626.
    • (2011) Angew. Chem. , vol.123 , pp. 7626
  • 39
    • 0026768573 scopus 로고
    • N-Tosylhydrazones bearing an electron-withdrawing group at the a position can be decomposed under milder conditions; see: a) A. Ouihia, L. René, B. Badet, Tetrahedron Lett. 1992, 33, 5509;
    • (1992) Tetrahedron Lett. , vol.33 , pp. 5509
    • Ouihia, A.1    René, L.2    Badet, B.3
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.