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Volumn 60, Issue 4, 1995, Pages 931-940

Reactions of Chiral Phosphorous Acid Diamides: The Asymmetric Synthesis of Chiral αpha;-Hydroxy Phosphonamides, Phosphonates, and Phosphonic Acids

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHONIC ACID DERIVATIVE;

EID: 0028857994     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00109a025     Document Type: Article
Times cited : (152)

References (65)
  • 12
    • 0027231045 scopus 로고
    • and references cited therein
    • Öhler, E.; Kotzinger, S. Synthesis 1993, 497 and references cited therein.
    • (1993) Synthesis , pp. 497
    • Öhler, E.1    Kotzinger, S.2
  • 33
    • 84912984992 scopus 로고
    • University of Missouri-St. Louis De la Cruz, A.; Koeller, K. J.; Rath, N. P.; Spilling, C. D. To be submitted for publication
    • Koeller, K. J., PhD Thesis, University of Missouri-St. Louis, 1993. De la Cruz, A.; Koeller, K. J.; Rath, N. P.; Spilling, C. D. To be submitted for publication.
    • (1993) PhD Thesis
    • Koeller, K.J.1
  • 39
    • 85022736967 scopus 로고    scopus 로고
    • Direct analysis on a ChiralPak AS column: EtOH-hexanes, (9:1 or 2:8), 1 ml/min, detection at 254nm for phosphonates 5b and 5c, and using a differential refractometer for phosphonate 5a. The order of elution was the R enantiomer followed by the S enantiomer in all three examples submitted
    • Direct analysis on a ChiralPak AS column: EtOH-hexanes, (9:1 or 2:8), 1 ml/min, detection at 254nm for phosphonates 5b and 5c, and using a differential refractometer for phosphonate 5a. The order of elution was the R enantiomer followed by the S enantiomer in all three examples. Kozlowski, J. K. Rath, N. P.; Spilling, C. D. Tetrahedron, submitted.
    • Tetrahedron
    • Kozlowski, J.K.1    Rath, N.P.2    Spilling, C.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.