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Volumn 354, Issue 16, 2012, Pages 2921-2927

Asymmetric intramolecular C-H insertion of α-diazoacetamides in water by dirhodium(II) catalysts derived from natural amino acids

Author keywords

diazo compounds; lactams; C H insertion; dirhodium(II); water

Indexed keywords


EID: 84869051878     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201200101     Document Type: Article
Times cited : (29)

References (60)
  • 39
    • 24044470646 scopus 로고    scopus 로고
    • C. J. Li, Chem. Rev. 2005, 105, 3095-3165
    • (2005) Chem. Rev. , vol.105 , pp. 3095-3165
    • Li, C.J.1
  • 47
    • 84869023556 scopus 로고    scopus 로고
    • [15] was reported to be around 2.38-2.41 Å while in the case of 7a-c, with water molecules at both coordination sites it was determined to be in the range 2.47-2.49 Å. The increase in Rh-Rh bond distance should be related with the lantern structure loss of the new complexes. CCDC 864696, CCDC 765711 and CCDC 765710 contains the supplementary crystallographic data for this paper (structures of 7a, 7b and 7c, respectively). These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 60
    • 79951663273 scopus 로고    scopus 로고
    • For a recent study on the use of intramolecular C-H insertion of α-diazo phosphonates:, J. Wang, V. Boyarskikh, J. D. Rainier, Org. Lett. 2011, 13, 700-702.
    • (2011) Org. Lett. , vol.13 , pp. 700-702
    • Wang, J.1    Boyarskikh, V.2    Rainier, J.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.