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Volumn 37, Issue 31, 1996, Pages 5593-5596

N-(chloromethyloxycarbonyl)pyrrolidine as a source of the HOCH2- synthon

Author keywords

[No Author keywords available]

Indexed keywords

ALKANEDIOL DERIVATIVE; CARBAMIC ACID DERIVATIVE; PYRROLIDINE DERIVATIVE;

EID: 0030605836     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01133-1     Document Type: Article
Times cited : (10)

References (39)
  • 1
    • 0004111873 scopus 로고
    • Hase, T. A. Ed.; John Wiley & Sons: New York
    • 1. For a review, see: Saavedra, J. E. In Umpoled Synthons, Hase, T. A. Ed.; John Wiley & Sons: New York, 1987; pp. 101-143.
    • (1987) Umpoled Synthons , pp. 101-143
    • Saavedra, J.E.1
  • 3
    • 0000084040 scopus 로고
    • 3. For a review on functionalised organolithium compounds, see: Nájera, C.; Yus, M. Trends Org. Chem. 1991, 2, 155-181.
    • (1991) Trends Org. Chem. , vol.2 , pp. 155-181
    • Nájera, C.1    Yus, M.2
  • 4
    • 5044246846 scopus 로고
    • 4. See, for instance: Still, W. C. J. Am. Chem. Soc. 1978, 100, 1481-1487.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 1481-1487
    • Still, W.C.1
  • 26
    • 0001262307 scopus 로고    scopus 로고
    • (c) For the last paper from our laboratory on the use of an arenecatalysed lithiation, see: Almena, J.; Foubelo, F.; Yus, M. J. Org. Chem. 1996, 61, 1859-1862.
    • (1996) J. Org. Chem. , vol.61 , pp. 1859-1862
    • Almena, J.1    Foubelo, F.2    Yus, M.3
  • 36
    • 85030200986 scopus 로고    scopus 로고
    • note
    • 2CO) the temperature was kept at -78°C during 1 h before the hydrolysis step.
  • 38
    • 85030208709 scopus 로고    scopus 로고
    • note
    • f= 0.35 (silica gel, hexane/ethyl acetate: 1/1 ).
  • 39
    • 85030197962 scopus 로고    scopus 로고
    • note
    • 16. In other examples for the transformation 2→3 carried out in our laboratory we obtained yields better than 90%. These results are in good agreement with the literature data (ref 10b).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.