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Volumn 29, Issue 12, 1990, Pages 1422-1424

Chiral Lithium‐1‐oxyalkanides by Asymmetric Deprotonation; Enantioselective Synthesis of 2‐Hydroxyalkanoic Acids and Secondary Alkanols

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Indexed keywords


EID: 0343583098     PISSN: 05700833     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.199014221     Document Type: Article
Times cited : (256)

References (41)
  • 4
    • 84990131806 scopus 로고    scopus 로고
    • At high temperature Wittig rearrangements occur
  • 31
    • 0000163012 scopus 로고
    • Die Homoaldol-Reaktion oder wie man Probleme der Regio- und Stereoselektivität in den Griff bekommt
    • Review
    • (1984) Angewandte Chemie , vol.96 , pp. 930-946
    • Hoppe, D.1
  • 33
    • 84990082552 scopus 로고    scopus 로고
    • All the new compounds gave correct elemental analyses (C, H ± 0.3%)
  • 35
    • 0025273372 scopus 로고
    • During the preparation of the manuscript a paper concerning the carboxylation of enantiomerically enriched α‐(benzyloxymethyl)alkanides of the type 4b appeared in the literature
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1985-1988
    • Chan, P.C.‐M.1    Chong, J.M.2
  • 36
    • 84990072708 scopus 로고    scopus 로고
    • Correlated as 14b‐methyl ester with a sample obtained from (R)‐lactic acid.
  • 37
    • 84990145031 scopus 로고    scopus 로고
    • 3. on a 300 MHz spectrometer on the basis of the α‐H signal. The absorption bands are in each case doubled, due to amide‐E/Z isomerism. The enantiomeric(S)‐14 methyl esters were not detectable in any of the samples.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.