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Volumn 76, Issue 2, 2011, Pages 728-731

Oxidation of α-oxo-oximes to nitrile oxides with hypervalent iodine reagents

Author keywords

[No Author keywords available]

Indexed keywords

[CARBONYL; ALDOXIMES; GOOD YIELD; HYPERVALENT IODINE REAGENTS; KETOXIMES; NITRILE OXIDES; NORBORNENES; OXIDATIVE CLEAVAGES;

EID: 78651517867     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo102241s     Document Type: Article
Times cited : (72)

References (50)
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    • Monograph: Hypervalent Iodine in Organic Synthesis; Academic Press: San Diego, CA, 1997
    • Wirth, T. Angew. Chem., Int. Ed. 2005, 44, 3656 Monograph: Varvoglis, A. Hypervalent Iodine in Organic Synthesis; Academic Press: San Diego, CA, 1997.
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 3656
    • Wirth, T.1    Varvoglis, A.2
  • 12
    • 77953298458 scopus 로고    scopus 로고
    • (PhI(OH)OTs). These techniques, however, are unsuitable for the conduct of tandem oxidative amidation/intramolecular nitrile oxide cycloaddition sequences (see text and ref 6)
    • Raihan, M. J.; Kavala, V.; Kuo, C.-W.; Rama Raju, B.; Yao, C. F. Green Chem. 2010, 12, 1090 (PhI(OH)OTs). These techniques, however, are unsuitable for the conduct of tandem oxidative amidation/intramolecular nitrile oxide cycloaddition sequences (see text and ref 6)
    • (2010) Green Chem. , vol.12 , pp. 1090
    • Raihan, M.J.1    Kavala, V.2    Kuo, C.-W.3    Rama Raju, B.4    Yao, C.F.5
  • 23
    • 35548985408 scopus 로고    scopus 로고
    • See especially pp 12255-12259
    • Nair, V.; Suja, T. D. Tetrahedron 2007, 63, 12247. See especially pp 12255-12259.
    • (2007) Tetrahedron , vol.63 , pp. 12247
    • Nair, V.1    Suja, T.D.2
  • 24
    • 70349906431 scopus 로고    scopus 로고
    • 4736. The methodology also enables the conduct of oxidative phenolic alkoxylation/INOC sequences
    • Mendelsohn, B. A.; Ciufolini, M. A. Org. Lett. 2009, 11, 4736. The methodology also enables the conduct of oxidative phenolic alkoxylation/INOC sequences
    • (2009) Org. Lett. , vol.11
    • Mendelsohn, B.A.1    Ciufolini, M.A.2
  • 30
    • 85065065911 scopus 로고
    • Reviews on bimolecular nitrile oxide cycloadditions and synthetic applications thereof
    • Reviews on bimolecular nitrile oxide cycloadditions and synthetic applications thereof: Grundmann, C. Synthesis 1970, 344
    • (1970) Synthesis , pp. 344
    • Grundmann, C.1
  • 39
    • 78651504831 scopus 로고    scopus 로고
    • Commercially available
    • Commercially available.
  • 41
    • 78651520901 scopus 로고    scopus 로고
    • Prepared according to: US 19610919 (CAS No. 61:83839). Details are provided as Supporting Information
    • Prepared according to: Werber, F. X. US 19610919 (CAS No. 61:83839). Details are provided as Supporting Information.
    • Werber, F.X.1
  • 46
    • 0000604457 scopus 로고    scopus 로고
    • Prepared according to
    • Prepared according to: Zolfigol, M. A. Molecules 2001, 6, 694
    • (2001) Molecules , vol.6 , pp. 694
    • Zolfigol, M.A.1
  • 47
    • 78651473394 scopus 로고    scopus 로고
    • Because of such poor yields, compounds 29 and 30 were not fully characterized
    • Because of such poor yields, compounds 29 and 30 were not fully characterized.
  • 50
    • 78651513225 scopus 로고    scopus 로고
    • Experimental protocols are provided as Supporting Information
    • Experimental protocols are provided as Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.