Synthetic studies on lepadiformine using the 2-azaallyl anion method

Journal of Organic Chemistry

Volumn 64, Issue 3, 1999, Pages 688-689

  Pearson, William H ^a   Ren, Yi ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2,13 DIEPILEPADIFORMINE; ALKALOID; ALLYL COMPOUND; ANION; UNCLASSIFIED DRUG;

ARTICLE; DIASTEREOISOMER; DRUG SYNTHESIS; REACTION ANALYSIS;

EID: 0033524891     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo982120j     Document Type: Article

References (12)

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2. (a) Blackman, A. J.; Li, C.; Hockless, D. C. R.; Skelton, B. W.; White, A. H. Tetrahedron 1993, 49, 8645-8656.
3. (b) Li, C.; Blackman, A. J. Aust. J. Chem. 1994, 47, 1355-1361.
4. (c) Li, C.; Blackman, A. J. Aust. J. Chem. 1995, 48, 955-965.
5. Patil, A. D.; Freyer, A. J.; Reichwein, R.; Carte, B.; Killmer, L. B.; Faucette, L.; Johnson, R. K. Tetrahedron Lett. 1997, 38, 363-364.
6. Pearson, W. H.; Barta, N. S.; Kampf, J. W. Tetrahedron Lett. 1997, 38, 3369-3372.
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9. Pearson, W. H.; Szura, D. P.; Postich, M. J. J. Am. Chem. Soc. 1992, 114, 1329-1345.
10. We thank Professor Biard for a sample of natural lepadiformine and for helpful discussions regarding its isolation and manipulation.
11. Marshall, J. A.; Garofalo, A. W. J. Org. Chem. 1993, 58, 3675-3680.
12. 13C NMR spectra of 27 and 1 are very different.