메뉴 건너뛰기




Volumn 352, Issue 14-15, 2010, Pages 2588-2598

One-pot synthesis of symmetrical 1,3-diarylureas or substituted benzamides directly from benzylic primary alcohols and effective oxidation of secondary alcohols to ketones using phenyliodine diacetate in combination with sodium azide

Author keywords

1,3 diarylureas; alcohols; hypervalent compounds; phenyliodine diacetate; sodium azide

Indexed keywords


EID: 78349266796     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000318     Document Type: Article
Times cited : (49)

References (104)
  • 38
    • 77149146146 scopus 로고    scopus 로고
    • for reviews or books on hypervalent iodine reagents, see
    • J. Yu, J. Tian, C. Zhang, Adv. Synth. Catal. 2010, 352, 531; for reviews or books on hypervalent iodine reagents, see
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 531
    • Yu, J.1    Tian, J.2    Zhang, C.3
  • 43
    • 0013167416 scopus 로고    scopus 로고
    • (Ed.: T. Wirth), Springer-Verlag, Berlin, Heidelberg
    • Hypervalent Iodine Chemistry, (Ed.:, T. Wirth,), Springer-Verlag, Berlin, Heidelberg, 2003
    • (2003) Hypervalent Iodine Chemistry
  • 57
    • 78349246923 scopus 로고    scopus 로고
    • For applications of urea derivatives, see
    • For applications of urea derivatives, see
  • 76
    • 78349241234 scopus 로고    scopus 로고
    • 2 which was essential for the transformation of benzaldehyde to 1,3-diphenylurea or benzamide via benzoyl azide.
    • 2 which was essential for the transformation of benzaldehyde to 1,3-diphenylurea or benzamide via benzoyl azide.
  • 77
    • 78349253240 scopus 로고    scopus 로고
    • Acetoxy and azide anions were analyzed quantitatively using a Dionex DX-120 Ion Chromatography System.
    • Acetoxy and azide anions were analyzed quantitatively using a Dionex DX-120 Ion Chromatography System.
  • 81
    • 24044531286 scopus 로고    scopus 로고
    • for examples on conversion of carbamoyl azides to primary amines under basic conditions, see
    • Angew. Chem. Int. Ed. 2005, 44, 5188; for examples on conversion of carbamoyl azides to primary amines under basic conditions, see
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5188
  • 83
    • 2842567310 scopus 로고
    • for reactions of carbamoyl azides with primary amines to form urea derivatives, see
    • E. Oliveri-Mandala, F. Noto, Gazz. Chim. Ital. 1913, 43, 514; for reactions of carbamoyl azides with primary amines to form urea derivatives, see
    • (1913) Gazz. Chim. Ital. , vol.43 , pp. 514
    • Oliveri-Mandala, E.1    Noto, F.2
  • 86
    • 78349266652 scopus 로고    scopus 로고
    • For the Curtius rearrangement of acyl azides, see
    • For the Curtius rearrangement of acyl azides, see
  • 90
    • 33947301041 scopus 로고
    • for the decomposition of acyl azides to acylnitrenes or amides, see
    • G. Ľabbé, Chem. Rev. 1969, 69, 345; for the decomposition of acyl azides to acylnitrenes or amides, see
    • (1969) Chem. Rev. , vol.69 , pp. 345
    • Ľabbé, G.1
  • 94
    • 78349274195 scopus 로고    scopus 로고
    • For the conversion of amides to isocyanates using hypervalent iodine reagents, see
    • For the conversion of amides to isocyanates using hypervalent iodine reagents, see
  • 99
    • 71949124406 scopus 로고    scopus 로고
    • for one report describing the synthesis of symmetrical 1,3-disubstitued ureas from amides during the preparation of the present manuscript, see
    • Angew. Chem. Int. Ed. 2009, 48, 9693; for one report describing the synthesis of symmetrical 1,3-disubstitued ureas from amides during the preparation of the present manuscript, see
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9693
  • 101
    • 0035802890 scopus 로고    scopus 로고
    • For an excellent review on selective oxidation of secondary alcohols, see.
    • For an excellent review on selective oxidation of secondary alcohols, see:, J. B. Arterburn, Tetrahedron 2001, 57, 9765.
    • (2001) Tetrahedron , vol.57 , pp. 9765
    • Arterburn, J.B.1
  • 104
    • 78349238341 scopus 로고    scopus 로고
    • Aldrich/ACD Library of FT NMR Spectra.
    • Aldrich/ACD Library of FT NMR Spectra.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.