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Volumn 38, Issue 7, 1997, Pages 1195-1196

A chemoenzymatic strategy for the synthesis of enantiopure (R)-(-)-baclofen

Author keywords

[No Author keywords available]

Indexed keywords

BACLOFEN;

EID: 0031575602     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00062-2     Document Type: Article
Times cited : (88)

References (15)
  • 10
    • 0011473944 scopus 로고    scopus 로고
    • note
    • -1.
  • 11
    • 37049071940 scopus 로고
    • Some modifications in the procedure allowed us to synthesize a 10 g scale of cyclobutanone 3 in 65% yield from 4-chlorostyrene 2 as starting material
    • 7. Kaiwar V., Reese C. B., Gray E. J., Neidle S. J. Chem. Soc., Perkin Trans. 1, 1995, 2281-2287. Some modifications in the procedure allowed us to synthesize a 10 g scale of cyclobutanone 3 in 65% yield from 4-chlorostyrene 2 as starting material.
    • (1995) J. Chem. Soc., Perkin Trans. 1 , pp. 2281-2287
    • Kaiwar, V.1    Reese, C.B.2    Gray, E.J.3    Neidle, S.4
  • 12
    • 0011426840 scopus 로고    scopus 로고
    • R = 26.8 min
    • R = 26.8 min.
  • 14
    • 0011383361 scopus 로고    scopus 로고
    • 25 = -39 (c = 1.0, EtOH)
    • 25 = -39 (c = 1.0, EtOH).
  • 15
    • 0011472114 scopus 로고    scopus 로고
    • 3)
    • 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.