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Volumn , Issue 21, 2007, Pages 2107-2120

Novel synthetic strategies for the preparation of prostacyclin and prostaglandin analogues - Off the beaten track

Author keywords

[No Author keywords available]

Indexed keywords

BENZOIC ACID; CARBACYCLIN; ISOCARBACYCLIN; ISOPROSTANE; LACTONE DERIVATIVE; PROSTACYCLIN; PROSTAGLANDIN DERIVATIVE;

EID: 34548349189     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b617693n     Document Type: Review
Times cited : (10)

References (180)
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    • (1979) Prostacyclin, Ed.
  • 9
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    • H. Wise and R. L. Jones, Kluwer Academic Publishers, New York
    • Prostacyclin and its Receptors, ed., H. Wise, and, R. L. Jones,, Kluwer Academic Publishers, New York, 2000
    • (2000) Prostacyclin and Its Receptors, Ed.
  • 44
    • 34548349156 scopus 로고    scopus 로고
    • Prostacyclin numbering
    • Prostacyclin numbering
  • 66
    • 34548331936 scopus 로고    scopus 로고
    • Prepared from commerically available 1,5-pentanediol in three steps
    • Prepared from commerically available 1,5-pentanediol in three steps
  • 98
    • 2742524363 scopus 로고
    • 13C NMR data for 15-deoxy-TIC (8), allowing for a better comparison than with the originally published 270 MHz data - see ref. 12
    • R. Mahrwald H. Schick K. K. Pivnitsky J. Prakt. Chem. 1990 332 403
    • (1990) J. Prakt. Chem. , vol.332 , pp. 403
    • Mahrwald, R.1    Schick, H.2    Pivnitsky, K.K.3
  • 101
    • 33750526047 scopus 로고    scopus 로고
    • 13C NMR spectral data and optical rotations for isocarbacyclin (6), 15R-TIC (9), are concurrent with literature values: For isocarbacyclin (6):
    • N. A. Sheddan J. Mulzer Org. Biomol. Chem. 2006 4 4127
    • (2006) Org. Biomol. Chem. , vol.4 , pp. 4127
    • Sheddan, N.A.1    Mulzer, J.2
  • 106
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    • Dipentyl zinc reagents 62 and 63 were prepared from their parent Grignard compound by the procedure outlined in ref. 40
    • T. O. Schrader M. L. Snapper Tetrahedron Lett. 2000 41 9685
    • (2000) Tetrahedron Lett. , vol.41 , pp. 9685
    • Schrader, T.O.1    Snapper, M.L.2
  • 107
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    • 1H NMR
    • 1H NMR
  • 111
    • 34548319425 scopus 로고    scopus 로고
    • For isocarbacyclin: diastereoselectivities were lower than with Ti-TADDOL complexes, and for 15R-TIC: either no reaction was observed or only that with poor yield and/or diastereoselectivity For lead references and recent reviews on cross metathesis, see:
    • For isocarbacyclin: diastereoselectivities were lower than with Ti-TADDOL complexes, and for 15R-TIC: either no reaction was observed or only that with poor yield and/or diastereoselectivity
  • 133
    • 0014219646 scopus 로고
    • For lead references and recent reviews, see:
    • S. Bergström Science 1967 157 382
    • (1967) Science , vol.157 , pp. 382
    • Bergström, S.1
  • 159
  • 171
  • 178
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    • 13C NMR spectral data and optical rotations for PGF2α (75) are concurrent with literature values found in ref. 57
    • N. A. Sheddan J. Mulzer Tetrahedron Lett. 2006 47 6689
    • (2006) Tetrahedron Lett. , vol.47 , pp. 6689
    • Sheddan, N.A.1    Mulzer, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.