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Volumn 52, Issue 2, 2004, Pages 214-220
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A synthesis of heteroaromatic analogues of 1-methyl-1,2,3,4- tetrahydroisoquinoline using the pummerer-type cyclization reaction: Observation of tandem cyclization reaction
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Author keywords
11 aza 2 oxa 7 thiatricyclo 4.3.3.01,5 dodecane; Benzofuro 2,3 c pyridine; Benzothieno 2,3 c pyridine; Pummerer reaction; Thieno 2,3 c pyridine
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Indexed keywords
1 METHYL 1,2,3,4 TETRAHYDROISOQUINOLINE DERIVATIVE;
1,2,3,4 TETRAHYDRO 1 METHYL 4 PHENYLSULFANYLBENZO[4,5]FURO[2,3 C]PYRIDINE 2 CARBALDEHYDE;
11 AZA 2 OXA 7 THIATRICYCLO[4.3.3.0 1,5 ]DODECANE;
19 FORMYL 18 METHYL 19 AZA 2 OXA 11 THIAPENTACYCLO[8.7.3.0 1,9 .0 3,8 .0 12,17 ]ICOSA 3,5,7,12,14,16 HEXENE;
4,5,6,7 TETRAHYDRO 7 METHYL 4 PHENYLSULFANYLTHIENO[2,3 C]PYRIDINE 6 CARBALDEHYDE;
ALDEHYDE DERIVATIVE;
ALKANE DERIVATIVE;
BENZOFURAN DERIVATIVE;
BENZOTHIOPHENE;
BENZOTHIOPHENE DERIVATIVE;
ISOQUINOLINE DERIVATIVE;
NITROGEN;
OXONIC ACID;
SULFOXIDE;
THIOPHENE;
TRIFLUOROACETIC ACID;
UNCLASSIFIED DRUG;
1 METHYL 1,2,3,4 TETRAHYDROISOQUINOLINE;
1-METHYL-1,2,3,4-TETRAHYDROISOQUINOLINE;
TETRAHYDROISOQUINOLINE DERIVATIVE;
ALKYLATION;
ARTICLE;
CHEMICAL REACTION KINETICS;
CYCLIZATION;
DIASTEREOISOMER;
DRUG SYNTHESIS;
PUMMERER REACTION;
QUANTUM YIELD;
REACTION ANALYSIS;
ROOM TEMPERATURE;
CHEMICAL STRUCTURE;
CHEMISTRY;
HYDROLYSIS;
OXIDATION REDUCTION REACTION;
STEREOISOMERISM;
SYNTHESIS;
CYCLIZATION;
HYDROLYSIS;
MOLECULAR STRUCTURE;
OXIDATION-REDUCTION;
STEREOISOMERISM;
SULFOXIDES;
TETRAHYDROISOQUINOLINES;
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EID: 4444379637
PISSN: 00092363
EISSN: 13475223
Source Type: Journal
DOI: 10.1248/cpb.52.214 Document Type: Article |
Times cited : (6)
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References (17)
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