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Volumn 65, Issue 18, 2000, Pages 5837-5838

Solvent effects on the monobromination of α,ω-diols: A convenient preparation of ω-bromoalkanols

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; ALKANOL; BENZENE; CYCLOHEXANE; OCTANE; SOLVENT; TOLUENE;

EID: 0033833095     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo000291u     Document Type: Note
Times cited : (92)

References (21)
  • 5
    • 0342339175 scopus 로고    scopus 로고
    • note
    • A search of the Science Citation Index showed >50 citations for the years 1987-1996. Significantly, the vast majority of papers citing this article used the method reported to prepare bromo alcohols. During the same period, ∼50% of the 1d → 2d conversions reported used this method.
  • 6
    • 0342774146 scopus 로고    scopus 로고
    • See, for example: (a) Nakayama, T.; Mori, K. Liebigs Ann. / Recl. 1997, 839-843. (b) Kaiser, A.; Marazano, C.; Maier, M. J. Org. Chem. 1999, 64, 3778-3782. (c) Sharma, A.; Chattopadhyay, S. J. Org. Chem. 1998, 63, 6128-6131.
    • (1997) Liebigs Ann. / Recl. , pp. 839-843
    • Nakayama, T.1    Mori, K.2
  • 7
    • 0032927132 scopus 로고    scopus 로고
    • See, for example: (a) Nakayama, T.; Mori, K. Liebigs Ann. / Recl. 1997, 839-843. (b) Kaiser, A.; Marazano, C.; Maier, M. J. Org. Chem. 1999, 64, 3778-3782. (c) Sharma, A.; Chattopadhyay, S. J. Org. Chem. 1998, 63, 6128-6131.
    • (1999) J. Org. Chem. , vol.64 , pp. 3778-3782
    • Kaiser, A.1    Marazano, C.2    Maier, M.3
  • 8
    • 0032483560 scopus 로고    scopus 로고
    • See, for example: (a) Nakayama, T.; Mori, K. Liebigs Ann. / Recl. 1997, 839-843. (b) Kaiser, A.; Marazano, C.; Maier, M. J. Org. Chem. 1999, 64, 3778-3782. (c) Sharma, A.; Chattopadhyay, S. J. Org. Chem. 1998, 63, 6128-6131.
    • (1998) J. Org. Chem. , vol.63 , pp. 6128-6131
    • Sharma, A.1    Chattopadhyay, S.2
  • 15
    • 0006287509 scopus 로고
    • When toluene was used in place of benzene (with a Dean-Stark trap), good yields of bromo alcohols were obtained but were contaminated with ca. 9% dibromides. (a) Enders, D.; Bartzen, D. Liebigs Ann. Chem. 1991, 569-574.
    • (1991) Liebigs Ann. Chem. , pp. 569-574
    • Enders, D.1    Bartzen, D.2
  • 18
    • 0000252132 scopus 로고
    • See, for example: (a) McDougal, P. G.; Rico, J. G.; Oh, Y.-I.; Condon, B. D. J. Org. Chem. 1986, 51, 3388-3390. (b) Houille, O.; Schmittberger, T.; Uguen, D. Tetrahedron Lett. 1996, 37, 625-628.
    • (1986) J. Org. Chem. , vol.51 , pp. 3388-3390
    • McDougal, P.G.1    Rico, J.G.2    Oh, Y.-I.3    Condon, B.D.4
  • 19
    • 0030065709 scopus 로고    scopus 로고
    • See, for example: (a) McDougal, P. G.; Rico, J. G.; Oh, Y.-I.; Condon, B. D. J. Org. Chem. 1986, 51, 3388-3390. (b) Houille, O.; Schmittberger, T.; Uguen, D. Tetrahedron Lett. 1996, 37, 625-628.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 625-628
    • Houille, O.1    Schmittberger, T.2    Uguen, D.3
  • 20
    • 0343644377 scopus 로고    scopus 로고
    • note
    • 3NCl or Aliquat 336 to these reactions did not affect product distributions, suggesting that aqueous solubility is not a significant issue here.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.