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Volumn 7, Issue 13, 2005, Pages 2715-2718

Syntheses of ficuseptine, juliprosine, and juliprosopine by biomimetic intramolecular chichibabin pyridine syntheses

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; FICUSEPTINE B; INDOLIZINE DERIVATIVE; JULIFLORINE; JULIPROSINE; PHENANTHRENE DERIVATIVE; PYRIDINE; PYRIDINE DERIVATIVE;

EID: 26844573545     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol050931l     Document Type: Article
Times cited : (50)

References (51)
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    • For leading references from 2002 to 2004, see: (a) Singh, R.; Ghosh, S. K. Tetrahedron Lett. 2002, 43, 7711-7715.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 7711-7715
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    • 29844434685 scopus 로고    scopus 로고
    • note
    • 1,5
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    • (b) Pomerantz, M.; Liu, L.; Zhang, X. ARKIVOC 2003, Part xii, 119-137; http://www.arkat-usa.org/ark/journal/2003/I12_Shine/HS-830J/HS-830J.pdf;
    • (2003) ARKIVOC , Issue.12 PART , pp. 119-137
    • Pomerantz, M.1    Liu, L.2    Zhang, X.3
  • 33
    • 29844436858 scopus 로고    scopus 로고
    • Chem. Abstr. 2004, 141, 55000k.
    • (2004) Chem. Abstr. , vol.141
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    • note
    • 3c
  • 36
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    • note
    • Compounds 16 and 2 are mixtures of two diastereomers because 15 is racemic, although only a single enantiomer is drawn. Similarly, compounds 17c, 17t, 24c, and 24t are mixtures of four diastereomers. Only the relative stereochemistry within each of the three ring systems is specified.
  • 37
    • 0010401826 scopus 로고
    • Katritzky, A. R., Boulton, A. J., Eds.; Academic Press: New York
    • (a) Lyle, R. E.; Anderson, R. S. In Advances in Heterocyclic Chemistry; Katritzky, A. R., Boulton, A. J., Eds.; Academic Press: New York, 1966; Vol. 6, pp 45-93.
    • (1966) Advances in Heterocyclic Chemistry , vol.6 , pp. 45-93
    • Lyle, R.E.1    Anderson, R.S.2
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    • (b) Ferles, M.; Pliml, J. In Advances in Heterocyclic Chemistry; Katritzky, A. R., Boulton, A. J., Eds.; Academic Press: New York, 1970; Vol. 12, pp 43-101.
    • (1970) Advances in Heterocyclic Chemistry , vol.12 , pp. 43-101
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  • 45
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    • 8Me are 73.5, 33.5, and 18.4. These carbons are shifted upfield to 65.9, 29.5, and 18.3 in the cis isomer by gauche interactions: Ashweek, N. J.; Coldham, I.; Snowden, D. J.; Vennall, G. P. Chem. - Eur. J. 2002, 8, 195-207.
    • (2002) Chem. - Eur. J. , vol.8 , pp. 195-207
    • Ashweek, N.J.1    Coldham, I.2    Snowden, D.J.3    Vennall, G.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.