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Volumn 49, Issue 28, 2008, Pages 4378-4382

Expedient synthesis and solvent dependent oxidation behavior of a water-soluble IBX derivative

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOTEREPHTHALIC ACID; 2 IODOBENZOIC ACID; PHTHALIC ACID;

EID: 44649137331     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.05.017     Document Type: Article
Times cited : (39)

References (30)
  • 3
    • 9444221234 scopus 로고    scopus 로고
    • Schmalz H.G., and Wirth T. (Eds), Wiley-VCH, Weinheim
    • Wirth T. In: Schmalz H.G., and Wirth T. (Eds). Organic Synthesis Highlights V (2003), Wiley-VCH, Weinheim 144-150
    • (2003) Organic Synthesis Highlights V , pp. 144-150
    • Wirth, T.1
  • 4
    • 44649201335 scopus 로고    scopus 로고
    • Wirth, T. In Top. Curr. Chem.; Wirth, T. Ed. 2003, 224, pp 185-208.
    • Wirth, T. In Top. Curr. Chem.; Wirth, T. Ed. 2003, 224, pp 185-208.
  • 13
    • 0035803642 scopus 로고    scopus 로고
    • For solid-phase anchored IBX derivatives, see:
    • For solid-phase anchored IBX derivatives, see:. Mûlabaier M., and Giannis A. Angew. Chem., Int. Ed. 40 (2001) 4393-4394
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4393-4394
    • Mûlabaier, M.1    Giannis, A.2
  • 21
    • 0037087704 scopus 로고    scopus 로고
    • Iodine center in oxygen ligand appended IBX derivatives is known to be involved in oxidation of substrates via single electron transfer (SET) pathways, see:
    • Iodine center in oxygen ligand appended IBX derivatives is known to be involved in oxidation of substrates via single electron transfer (SET) pathways, see:. Nicolaou K.C., Montagnon T., and Baran P.S. Angew. Chem., Int. Ed. 41 (2002) 993-996
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 993-996
    • Nicolaou, K.C.1    Montagnon, T.2    Baran, P.S.3
  • 25
    • 0037743696 scopus 로고    scopus 로고
    • Relevant bond dissociation energies (BDE) used for comparing the relative ease of α-H abstraction from benzylic alcohol, non-benzylic alcohol, allylic alcohol and THF are 87.5 ± 1.6 kcal/mol, 93.7 ± 1.8 kcal/mol, 81.6 ± 1.8 kcal/mol, and 92.1 ± 1.6 kcal/ mol, respectively and the BDE values are compiled from:, CRC Press, Boca Raton, Florida
    • Relevant bond dissociation energies (BDE) used for comparing the relative ease of α-H abstraction from benzylic alcohol, non-benzylic alcohol, allylic alcohol and THF are 87.5 ± 1.6 kcal/mol, 93.7 ± 1.8 kcal/mol, 81.6 ± 1.8 kcal/mol, and 92.1 ± 1.6 kcal/ mol, respectively and the BDE values are compiled from:. Luo Y.-R. Handbook of Bond Dissociation Energies in Organic Compounds (2003), CRC Press, Boca Raton, Florida
    • (2003) Handbook of Bond Dissociation Energies in Organic Compounds
    • Luo, Y.-R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.