Formal synthesis of vallesamidine

Helvetica Chimica Acta

Volumn 89, Issue 2, 2006, Pages 249-257

  Ho, Tse Lok ^a,b   Chen, Chun Kuei ^a  

^a NATIONAL CHIAO TUNG UNIVERSITY   (Taiwan)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLATION; ISOMERS; OXIDATION; POTASSIUM COMPOUNDS; SELENIUM; SYNTHESIS (CHEMICAL);

BARTON DECARBOXYLATION; CYCLOHEPT-4-ENYL-1-CARBALDEHYDE; PICTET-SPENGLER REACTION; RACEMIC SELENIDES;

SELENIUM COMPOUNDS;

1 ETHYL 2,3,6,7,12,12B HEXAHYDRO 1 [2 (PHENYLSELENO)ETHYL]INDOLO[2,3 A]QUINOLIZIN 4(1H) ONE; ALDEHYDE DERIVATIVE; CYCLOHEPT 4 ENYL 1 CARBALDEHYDE; INDOLE ALKALOID; PERMANGANATE POTASSIUM; QUINAZOLINONE DERIVATIVE; SELENIDE; TRYPTAMINE; UNCLASSIFIED DRUG; VALLESAMIDINE;

ARTICLE; BARTON DECARBOXYLATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; DECARBOXYLATION; INFRARED SPECTROSCOPY; ISOMER; OXIDATION; PICTET SPENGLER REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 33644680678     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200690027     Document Type: Article

References (22)

1. G. Stork, Nature 1980, 284, 383;
2. T.-L. Ho, 'Tactics for Organic Synthesis', John Wiley & Sons, New York, 1994.
3. T.-L. Ho, R-F. Yang, Tetrahedron 1995, 51, 181.
4. T.-L, Ho, F.-S. Liang, Chem. Commun. 1996, 1887.
5. T.-L. Ho, R.-J. Chein, J. Nat. Prod. 1997, 60, 493.
6. T.-L, Ho, M.-H, Chang, J. Chem. Soc., Perkin Trans. 1 1999, 2479.
7. T.-L. Ho, G. H. Jana, J. Org. Chem. 1999, 64, 8965.
8. T.-L. Ho, E. Gorobets, Tetrahedron 2002, 58, 4969.
9. T.-L. Ho, E. V. Kuzakov, Helv. Chim. Acta 2004, 87, 2712.
10. T.-L. Ho, C.-K. Chen, Helv. Chim. Acta 2005, 88, 2764.
11. T.-L. Ho, 'Symmetry: A Basis for Synthesis Design', John Wiley & Sons, New York, 1995.
12. J. Harley-Mason, M. Kaplan, J. Chem. Soc., Chem. Commun. 1967, 915.
13. a) A. Walser, C. Djerassi, Helv. Chim. Acta 1965, 48, 391;
14. b) S. H. Brown, C. Djerassi, P. G. Simpson, J. Am. Chem. Soc. 1968, 90, 2445;
15. C. H. Heathcock, M. H. Norman, D. A. Dickman, J. Org. Chem. 1990, 55, 798;
16. H. Tanino, K. Fukuichi, M. Ushiyama, K. Okada, Tetrahedron 2004, 60, 3273.
17. G. Stork, H. K. Landesman, J. Am. Chem. Soc. 1956, 78, 5128.
18. H. Marschall, F. Vogel, P. Weyerstahl, Justus Liebigs Ann. Chem. 1977, 1557.
19. W. Jiang, X. Zhang, Z. Sui, Org. Lett. 2003, 5, 43.
20. M. E. Kuehne, J. Am. Chem. Soc. 1964, 86, 2946.
21. D. H. R. Barton, S. Z. Zard, Pure Appl. Chem. 1986, 58, 675;
22. D. P. Curran, Synthesis 1988, 489.