Chemistry of indoles carrying a basic function. Part VII. A new aspect of Stobbe reaction

Heterocycles

Volumn 60, Issue 2, 2003, Pages 309-319

  Moldvai, István ^a   Temesvári Major, Eszter ^a   Incze, Mária ^a   Platthy, Tünde ^a   Gács Baitz, Eszter ^a   Szántay, Csaba ^a  

^a CHEMICAL RESEARCH CENTER   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

1,2ALPHA DIMETHYL 3BETA HYDROXY 3ALPHA PHENYL 4BETA,5ALPHA DIETHOXYCARBONYLPIPERIDINE; 1,2ALPHA DIMETHYL 3BETA PHENYL 4BETA ETHOXYCARBONYLPYRROLIDINE 3ALPHA,4ALPHA BUTYROLACTONE; 1,2BETA DIMETHYL 3BETA HYDROXY 3ALPHA PHENYL 4BETA,5ALPHA DIETHOXYCARBONYLPIPERIDINE; 5 OXO 1,3,4,5 TETRAHYDROBENZ[C,D]INDOLE 4,6' SPIRO(1' METHYL 3' BETA ETHOXYCARBONYL 5' OXO)PIPERIDINE; 8BETA,9ALPHA DICARBOETHOXY 10ALPHA HYDROXYERGOLINE(5BETA H); ESTER DERIVATIVE; INDOLE DERIVATIVE; PIPERIDINE DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; DIASTEREOISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYMERIZATION; STEREOCHEMISTRY; STOBBE CONDENSATION; SYNTHESIS;

EID: 0037322978     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-02-9628     Document Type: Article

References (23)

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13. 3), 128.13, 130.19, 132.78 (C-aromatics), 136.28 (C-1′), 156.72 (C=N), 191.91 (C=O).
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15. 3), 23.24 (C-3), 50.03 (C-2), 128.68, 128.84, 133.81 (C-aromatics), 133.91 (C-1′), 169.92 (NHCO), 199.14 (C=O).
16. 3), 23.24 (C-3), 50.03 (C-2), 128.68, 128.84, 133.81 (C-aromatics), 133.91 (C-1′), 169.92 (NHCO), 199.14 (C=O).
17. 3), 50.79 (C-2), 128.74, 129.13 (C-2′, C-3′, C-5′, C-6′), 132.88 (C-1′), 134.42 (C-4′), 196.12 (C=O).
18. 3), 50.79 (C-2), 128.74, 129.13 (C-2′, C-3′, C-5′, C-6′), 132.88 (C-1′), 134.42 (C-4′), 196.12 (C=O).
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22. 3), 128.35, 128.46, 128.96 (C-aromatics), 138.70 (2xC-1′), 147.73 (C-3, C-6), 150.98 (C-2, C-5).
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