메뉴 건너뛰기




Volumn 10, Issue 3, 1999, Pages 511-517

New chiral β-diketones based on [2.2]paracyclophane

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BIS(4 [2.2]PARACYCLOPHANYL)PROPANE 1,3 DIONE; 4 ACETYL[2.2]PARACYCLOPHANE; [1 (4 [2.2]PARACYCLOPHANYL) 3 PHENYL]PROPANE 1,3 DIONE; CARBOXYLIC ACID DERIVATIVE; DIKETONE; ESTER DERIVATIVE; LITHIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033548177     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00021-X     Document Type: Article
Times cited : (18)

References (28)
  • 9
    • 0001638960 scopus 로고
    • Nakamura, A.; Konishi, A.; Tatsuno, Y.; Otsuka, S. J. Am. Chem. Soc. 1978, 100, 3443; 1978, 100, 3449; Nakamura, A. Pure Appl. Chem. 1978, 50, 37.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 3449
  • 10
    • 0001924364 scopus 로고
    • Nakamura, A.; Konishi, A.; Tatsuno, Y.; Otsuka, S. J. Am. Chem. Soc. 1978, 100, 3443; 1978, 100, 3449; Nakamura, A. Pure Appl. Chem. 1978, 50, 37.
    • (1978) Pure Appl. Chem. , vol.50 , pp. 37
    • Nakamura, A.1
  • 17
    • 0345351725 scopus 로고
    • Levine, R., Conroy, J. A.; Adams, J. T.; Houser, Ch. R. J. Am. Chem. Soc. 1945, 67, 1510; Bloomfield, J. J. J. Org. Chem. 1962, 27, 2742.
    • (1962) J. Org. Chem. , vol.27 , pp. 2742
    • Bloomfield, J.J.1
  • 19
    • 0345611266 scopus 로고    scopus 로고
    • note
    • Both enantiomers of 3 were converted into the corresponding methyl esters (S)- and (R)-2. The determination of their enantiomeric purity was performed with chiral HPLC on tris(3,5-dimethylphenyl)carbamate derivative of cellulose in Prof. F. Vögtle's laboratory (see Acknowledgements).
  • 21
    • 84981800009 scopus 로고
    • 2 as a reagent was reported earlier: (a) Falk, H.; Schlogl, K. Angew. Chem., Int. Ed. Engl. 1968, 7, 383; (b) Falk, H.; Reich-Rohrwig, P.; Schlogl, K. Tetrahedron 1970, 26, 511; (c) The synthesis of ketone 1 by the reaction of acid 3 with methyllithium as a reagent with 54% chemical yield was also described with reference to 14(b) but without any experimental details or synthetic technique disclosed, Delton, M. J.; Cram, D. J. J. Am. Chem. Soc. 1972, 94, 2471.
    • (1968) Angew. Chem., Int. Ed. Engl. , vol.7 , pp. 383
    • Falk, H.1    Schlogl, K.2
  • 22
    • 0000018043 scopus 로고
    • 2 as a reagent was reported earlier: (a) Falk, H.; Schlogl, K. Angew. Chem., Int. Ed. Engl. 1968, 7, 383; (b) Falk, H.; Reich-Rohrwig, P.; Schlogl, K. Tetrahedron 1970, 26, 511; (c) The synthesis of ketone 1 by the reaction of acid 3 with methyllithium as a reagent with 54% chemical yield was also described with reference to 14(b) but without any experimental details or synthetic technique disclosed, Delton, M. J.; Cram, D. J. J. Am. Chem. Soc. 1972, 94, 2471.
    • (1970) Tetrahedron , vol.26 , pp. 511
    • Falk, H.1    Reich-Rohrwig, P.2    Schlogl, K.3
  • 23
    • 0013398257 scopus 로고
    • 2 as a reagent was reported earlier: (a) Falk, H.; Schlogl, K. Angew. Chem., Int. Ed. Engl. 1968, 7, 383; (b) Falk, H.; Reich-Rohrwig, P.; Schlogl, K. Tetrahedron 1970, 26, 511; (c) The synthesis of ketone 1 by the reaction of acid 3 with methyllithium as a reagent with 54% chemical yield was also described with reference to 14(b) but without any experimental details or synthetic technique disclosed, Delton, M. J.; Cram, D. J. J. Am. Chem. Soc. 1972, 94, 2471.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 2471
    • Delton, M.J.1    Cram, D.J.2
  • 27
    • 0344749168 scopus 로고    scopus 로고
    • Canadian Patent 638.335 (1962)
    • (b) Gorham, W. F. Canadian Patent 638.335 (1962).
    • Gorham, W.F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.