메뉴 건너뛰기




Volumn 9, Issue 8, 2007, Pages 1517-1520

Synthesis of carbamates and ureas using Zr(IV)-catalyzed exchange processes

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; CARBAMIC ACID DERIVATIVE; CARBONIC ACID DERIVATIVE; UREA; ZIRCONIUM;

EID: 34247506339     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0702728     Document Type: Article
Times cited : (79)

References (49)
  • 8
    • 0040183791 scopus 로고    scopus 로고
    • For a review on the use of phosgene substitutes, see
    • For a review on the use of phosgene substitutes, see: Biggi, F.; Maggi, R.; Sartori, G. Green Chem. 2000, 2, 140.
    • (2000) Green Chem , vol.2 , pp. 140
    • Biggi, F.1    Maggi, R.2    Sartori, G.3
  • 10
    • 34247504644 scopus 로고    scopus 로고
    • For recent reviews on the chemistry of dialkyl carbonates, see: a
    • For recent reviews on the chemistry of dialkyl carbonates, see: (a) Shaikh, A.-A. G.; Sivaram, S. Chem. Rev. 1996, 96, 95).
    • (1996) Chem. Rev , vol.96 , pp. 95
    • Shaikh, A.-A.G.1    Sivaram, S.2
  • 11
    • 0034644564 scopus 로고    scopus 로고
    • 8207. For a review on the chemistry of dimethylcarbonate, see
    • (b) Parrish, J. P.; Salvatore, R. N.; Jung, K. W. Tetrahedron 2000, 56, 8207. For a review on the chemistry of dimethylcarbonate, see:
    • (2000) Tetrahedron , vol.56
    • Parrish, J.P.1    Salvatore, R.N.2    Jung, K.W.3
  • 13
    • 0037040487 scopus 로고    scopus 로고
    • 2: (a) Baba, T.; Fujiwara, M ; Oosaku, A.; Kobayashi, A.; Deleon, R. G.; Ono, Y. Appl. Catal., A 2002, 227, 1.
    • 2: (a) Baba, T.; Fujiwara, M ; Oosaku, A.; Kobayashi, A.; Deleon, R. G.; Ono, Y. Appl. Catal., A 2002, 227, 1.
  • 14
    • 0037043070 scopus 로고    scopus 로고
    • 3: (b) Curini, M.; Epifano, F.; Maltese, F.; Rosati, O. Tetrahedron Lett. 2002, 43, 4895.
    • 3: (b) Curini, M.; Epifano, F.; Maltese, F.; Rosati, O. Tetrahedron Lett. 2002, 43, 4895.
  • 15
    • 0742320252 scopus 로고    scopus 로고
    • 3: (c) Distaso, M.; Quaranta, E. Tetrahedron 2004, 60, 1531.
    • 3: (c) Distaso, M.; Quaranta, E. Tetrahedron 2004, 60, 1531.
  • 16
    • 0032514855 scopus 로고    scopus 로고
    • 4-n: (a) Chong, P. Y.; Janicki, S. Z.; Petillo, P. A. J. Org. Chem. 1998, 63, 8515.
    • 4-n: (a) Chong, P. Y.; Janicki, S. Z.; Petillo, P. A. J. Org. Chem. 1998, 63, 8515.
  • 17
    • 0034641469 scopus 로고    scopus 로고
    • 3: (b) Vauthey, I.; Valot, F.; Gozzi, C.; Fache, F.; Lemaire, M. Tetrahedron Lett. 2000, 41, 6347,
    • 3: (b) Vauthey, I.; Valot, F.; Gozzi, C.; Fache, F.; Lemaire, M. Tetrahedron Lett. 2000, 41, 6347,
  • 18
    • 0034685972 scopus 로고    scopus 로고
    • 2: (c) Gastaldi, S.; Weinreb, S. M.; Stien D. J. Org. Chem. 2000, 65, 3239.
    • 2: (c) Gastaldi, S.; Weinreb, S. M.; Stien D. J. Org. Chem. 2000, 65, 3239.
  • 19
    • 1642372112 scopus 로고    scopus 로고
    • 3 : (d) Lee, S.-H.; Matsushita, H.; Clapham, B.; Janda, K. D. Tetrahedron 2004, 60, 3439.
    • 3 : (d) Lee, S.-H.; Matsushita, H.; Clapham, B.; Janda, K. D. Tetrahedron 2004, 60, 3439.
  • 21
    • 0037467369 scopus 로고    scopus 로고
    • For recent reports on Ti-(IV)-catalyzed transamidation, see: (b) Eldred, S. E.; Stone, D. A.; Gellman, S. H.; Stahl, S. S. J. Am. Chem. Soc. 2003, 125, 3422.
    • For recent reports on Ti-(IV)-catalyzed transamidation, see: (b) Eldred, S. E.; Stone, D. A.; Gellman, S. H.; Stahl, S. S. J. Am. Chem. Soc. 2003, 125, 3422.
  • 23
    • 34247497278 scopus 로고    scopus 로고
    • See Supporting Information for complete experimental details
    • See Supporting Information for complete experimental details.
  • 24
    • 0002289488 scopus 로고    scopus 로고
    • For representative examples of metal complexes containing HYP or HYP derivatives, see: Cu, Ni, and Co: (a) Parsons, S.; Winpenny, R. E. P. Acc. Chem. Res. 1997, 30, 89.
    • For representative examples of metal complexes containing HYP or HYP derivatives, see: Cu, Ni, and Co: (a) Parsons, S.; Winpenny, R. E. P. Acc. Chem. Res. 1997, 30, 89.
  • 27
    • 33745911141 scopus 로고    scopus 로고
    • Ti and Zr: (d) Takashima, Y.; Nakayama, Y.; Hashiguchi, M.; Hosoda, T.; Yasuda, H.; Hirao, T.; Harada, A. Polymer 2006, 47, 5762.
    • Ti and Zr: (d) Takashima, Y.; Nakayama, Y.; Hashiguchi, M.; Hosoda, T.; Yasuda, H.; Hirao, T.; Harada, A. Polymer 2006, 47, 5762.
  • 29
    • 34247550308 scopus 로고    scopus 로고
    • For examples of MeHYQ-containing metal complexes, see: Li: (a) Liddle, S. T, Clegg, W. J. Chem. Soc, Dalton Trans. 2002, 3923
    • For examples of MeHYQ-containing metal complexes, see: Li: (a) Liddle, S. T.; Clegg, W. J. Chem. Soc., Dalton Trans. 2002, 3923.
  • 39
    • 34247463785 scopus 로고    scopus 로고
    • Troc = 2,2,2-trichloroethyloxycarbonyl. Alloc = allyloxycarbonyl, Cbz = ben/yloxycarbonyl. Boc = tert-butoxycarbonyl.
    • Troc = 2,2,2-trichloroethyloxycarbonyl. Alloc = allyloxycarbonyl, Cbz = ben/yloxycarbonyl. Boc = tert-butoxycarbonyl.
  • 40
    • 29144466640 scopus 로고    scopus 로고
    • For urea synthesis via high-pressure-promoted condensation of Troc carbamates and amines, see
    • For urea synthesis via high-pressure-promoted condensation of Troc carbamates and amines, see: Azad, S.; Kumanoto, K.; Uegaki, K.; Ichikawa, Y.; Kotsuki, H. Tetrahedron Lett. 2006, 47, 587.
    • (2006) Tetrahedron Lett , vol.47 , pp. 587
    • Azad, S.1    Kumanoto, K.2    Uegaki, K.3    Ichikawa, Y.4    Kotsuki, H.5
  • 41
    • 33947336563 scopus 로고    scopus 로고
    • For representative metal isocyanate complexes, see: Fe: (a) King, R. B.; Bisnette, M. B. Inorg. Chem. 1966, 5, 306.
    • For representative metal isocyanate complexes, see: Fe: (a) King, R. B.; Bisnette, M. B. Inorg. Chem. 1966, 5, 306.
  • 46
    • 0033171910 scopus 로고    scopus 로고
    • For zirconium-catalyzed condensation of isocyanates and alcohols, see
    • For zirconium-catalyzed condensation of isocyanates and alcohols, see: Blank, W. J.; He, Z. A.; Hessell, E. T. Prog. Org. Coat. 1999, 35, 19.
    • (1999) Prog. Org. Coat , vol.35 , pp. 19
    • Blank, W.J.1    He, Z.A.2    Hessell, E.T.3
  • 49
    • 0344887064 scopus 로고    scopus 로고
    • 2Et, 24.6. Bordwell, F. G. Acc. Chem. Res. 1988, 21, 456.
    • 2Et, 24.6. Bordwell, F. G. Acc. Chem. Res. 1988, 21, 456.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.