A short entry into the pyrido[2,3-b]indole ring system. Synthesis of the tetracyclic segment of the marine antitumor agents: Grossularines-1 and -2

Tetrahedron Letters

Volumn 34, Issue 13, 1993, Pages 2127-2130

  Achab, Saïd ^a,b   Guyot, Michéle ^a   Potier, Pierre ^a  

^a MUSÉUM NATIONAL D'HISTOIRE NATURELLE   (France)

^b UNIVERSITÉ DE REIMS CHAMPAGNE ARDENNE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; GROSSULARINE 2; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL;

EID: 0027406260     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)60362-3     Document Type: Article

References (25)

1. Syntheses of functionalised pyrido[2,3-b]indoles
2. Conjugated heterocumulenes. Synthesis of conjugated carbodiimides and their facile conversion via intramolecular cycloaddition into nitrogen heterocycles, quinoline and pyrido[2,3-b]indole (?-carboline) derivatives
3. Reactions of ethyl 3-ethoxymethylene-2,4-dioxovalerate and ethyl ethoxymethyleneoxaloacetate with indole analogs.
4. Improved synthesis of 2,3-disubstituted pyridines by metallation of 2-chloropyridine: a convenient route to fused polyheterocycles
5. Directed ortho-lithiation of chloroquinolines. Application to synthesis of 2,3-disubstituted quinolines
6. Synthesis of isoascididemin, a regioisomer of the marine alkaloid ascididemin
7. Titanium (O) Reagents; 4. A selective and efficient reduction of nitropyridine derivatives
8. The synthesis of various chloroimidazo[4,5-c]pyridines and related derivatives
9. The Chemistry of Dichloromethylenammonium Salts (?Phosgenimonium Salts?)
10. Palladium-catalyzed cross-coupling reactions of highly hindered, electron-rich phenol triflates and organostannanes