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Volumn 43, Issue 19, 2002, Pages 3593-3596

Desymmetrisation of dialdehydes: (+)-(S) and (-)-(R) nor-methyl mevaldate as versatile synthetic intermediates

Author keywords

3 (t butyldimethylsilyloxy)pentanedial; Desymmetrisation; Nor methyl mevaldate

Indexed keywords

3 (TERT BUTYLDIMETHYLSILYLOXY)PENTANEDIAL; ALDEHYDE DERIVATIVE; METHYL GROUP; NORMEVALDATE; PHENETHYL ALCOHOL; UNCLASSIFIED DRUG;

EID: 0037029773     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)00533-6     Document Type: Article
Times cited : (8)

References (35)
  • 29
    • 0008819281 scopus 로고    scopus 로고
    • Leaving the reaction for longer times led to no increase in conversion, but the diastereoisomeric ratios on the isolated products are lower.
  • 30
    • 0008818943 scopus 로고    scopus 로고
    • note
  • 31
    • 0008841150 scopus 로고    scopus 로고
    • note
  • 32
    • 0008868252 scopus 로고    scopus 로고
    • 3), Ref. 5.
  • 33
    • 0008848238 scopus 로고    scopus 로고
    • 4 and the solvent was removed under reduced pressure to give a crude reaction product (25 mg), which was purified by column chromatography to give (R)-1 (13 mg, 76%) and (R)-2-phenylethanol (5 mg, 64%).
  • 34
    • 0008848928 scopus 로고    scopus 로고
    • 3) -4.48, -4.40, 17.81 25.56, 42.30, 50.84, 51.37, 64.99, 170.95, 200.35.
  • 35
    • 0008822627 scopus 로고    scopus 로고
    • Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 168527 and 168528. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: +44(0)-1223-336033; e-mail: deposit@ccdc.cam.ac.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.