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Volumn 50, Issue 5-6, 2007, Pages 290-294
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Mechanism of the Bischler-Napieralski exocyclic and endocyclic dehydration products in the radiosynthesis of (R)-(-)-(6a-14C)apomorphine
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Author keywords
Apomorphine; Bischler Napieralski; Cyclodehydration; Endocyclic; Exocyclic
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Indexed keywords
CHLORINE COMPOUNDS;
2-NITROBENZYL;
APOMORPHINE;
BISCHLE-NAPIERALSKI;
CARBON 14;
CYCLODEHYDRATION;
ENDOCYCLIC;
EXOCYCLIC;
ISOQUINOLINES;
RADIOSYNTHESIS;
REFLUXING;
DEHYDRATION;
1 (3,4 DIMETHOXY 2 NITROBENZAL) 1,2,3,4 TETRAHYDRO[1]ISOQUINOLINE C 14;
1 (3,4 DIMETHOXY 2 NITROBENZYL)DIHYDRO[1]ISOQUINOLINE C 14;
3 (6,7 DIMETHOXYANTHRANIL) DIHYDRO[1]ISOQUINOLINE C 14;
3,4 DIMETHOXY 2 NITROPHENYL N PHENETHYL[CARBOXYL]ACETAMIDE C 14;
3,4 DIMETHOXY 2 NITROPHENYL N PHENETHYL[CARBOXY]ACETAMIDE C 14;
6A APOMORPHINE C 14;
ACETAMIDE DERIVATIVE;
APOMORPHINE;
ISOQUINOLINE;
UNCLASSIFIED DRUG;
CONFERENCE PAPER;
DRUG STRUCTURE;
DRUG SYNTHESIS;
MASS SPECTROMETRY;
PROTON NUCLEAR MAGNETIC RESONANCE;
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EID: 34548159989
PISSN: 03624803
EISSN: 10991344
Source Type: Journal
DOI: 10.1002/jlcr.1270 Document Type: Conference Paper |
Times cited : (1)
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References (12)
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