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Volumn 53, Issue 13, 1997, Pages 4835-4856

α-Nitrogenated organolithium compounds from α-amidomethyl and α-aminomethyl sulfones

Author keywords

[No Author keywords available]

Indexed keywords

2 PYRROLIDONE DERIVATIVE; AMINOALCOHOL; CARBAMIC ACID DERIVATIVE; OXAZOLINE DERIVATIVE;

EID: 0030932870     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00166-X     Document Type: Article
Times cited : (31)

References (55)
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    • (c) For a recent review on arene-catalysed lithiation, see: Yus, M. Chem. Soc. Rev. 1996, 155-161.
    • (1996) Chem. Soc. Rev. , pp. 155-161
    • Yus, M.1
  • 15
    • 0000084040 scopus 로고
    • (b) 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
  • 16
    • 0343786778 scopus 로고    scopus 로고
    • note
    • To the best of our knowledge, only one example on the lithiation of a α-amido sulfone and the subsequent reaction with methyl iodide has been described (reference 1c).
  • 17
    • 0030590462 scopus 로고    scopus 로고
    • For recent leading references, see: (a) Park, Y. S: Beak, P. Tetrahedron 1996, 52, 12333-12350.
    • (1996) Tetrahedron , vol.52 , pp. 12333-12350
    • Park, Y.S.1    Beak, P.2
  • 22
    • 0342915916 scopus 로고    scopus 로고
    • See, for instance reference 1c
    • (a) See, for instance reference 1c.
  • 23
    • 0029994469 scopus 로고    scopus 로고
    • and references cited therein
    • (b) For a recent paper, see: Coldham, I.; Hutton, R.; Snowden, D. J. J. Am. Chem. Soc. 1996, 118, 5322-5323 and references cited therein.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 5322-5323
    • Coldham, I.1    Hutton, R.2    Snowden, D.J.3
  • 33
    • 0343786777 scopus 로고    scopus 로고
    • note
    • This compound was prepared by reaction of p-toluenesulfinic acid with aqueous formaldehyde and N-methylaniline in methanol in 80% yield (see reference 2).
  • 40
    • 0342915911 scopus 로고    scopus 로고
    • note
    • 2O content measured by gas chromatography) does not allow the determination of %D. Thus, calculated %H/D values are corrected considering this fact.
  • 42
    • 0342481642 scopus 로고    scopus 로고
    • note
    • + signal.
  • 44
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    • Malawska, B; Gorczyca, M. Acta Pol. Pharm. 1985, 42, 359-366; Chem. Abstr. 1987, 106, 18292p.
    • (1987) Chem. Abstr. , vol.106 , pp. 18292
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  • 54
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    • Tsujimoto, Y.; Nakahara, A.; Nishimura, Y.; Miyamoto, T.; Odaira, Y. Bull. Chem. Soc. Jpn. 1976, 49, 3705-3706; Chem. Abstr. 1977, 86, 155555j.
    • (1977) Chem. Abstr. , vol.86
  • 55
    • 0343786759 scopus 로고    scopus 로고
    • note
    • This work was supported by DGICYT from the Spanish Ministerio de Educación y Ciencia (MEC; projects no. PB94-1514 and PB94-1515). D. A. A., E. A. and D. J. R. thank the MEC for grants.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.