|
Volumn 67, Issue 3, 2011, Pages 655-659
|
Highly efficient one-pot synthesis of D-ring chloro-substituted neocryptolepines via a condensation - Pd-catalyzed intramolecular direct arylation strategy
|
Author keywords
C H Activation; Intramolecular direct arylation; Malaria; One pot
|
Indexed keywords
2,3 DIBROMO 1 METHYLPYRIDINIUMTRIFLUOROMETHANESULFONATE;
3 BROMO 2 CHLORO 1 METHYLQUINOLINIUM TRIFLATE;
3 BROMO 2 CHLORO 1 METHYLQUINOLINIUM TRIFLUOROMETHANESULFONATE;
3 BROMO 2 CHLOROQUINOLINE;
5 METHYL 5H INDOLO[2,3 B]QUINOLINE;
6 CHLORO 1 METHYL 1H PYRIDO[2,3 B]INDOLE;
7 CHLORO 1 METHYL 1H PYRIDO[2,3 B]INDOLE;
7 CHLORO 5 METHYL 5H INDOLO[2,3 B]QUINOLINE;
8 CHLORO 1 METHYL 1H PYRIDO[2,3 B]INDOLE;
8 CHLORO 5 METHYL 5H INDOLO[2,3 B]QUINOLINE;
9 CHLORO 5 METHYL 5H INDOLO[2,3 B]QUINOLINE;
ANTIMALARIAL AGENT;
N [3 BROMO 1 METHYLPYRIDIN 2(1H) YLIDENE] 2 CHLOROANILINE;
N [3 BROMO 1 METHYLPYRIDIN 2(1H) YLIDENE] 3 CHLOROANILINE;
N [3 BROMO 1 METHYLPYRIDIN 2(1H) YLIDENE] 4 CHLOROANILINE;
NEOCRYPTOLEPINE DERIVATIVE;
PALLADIUM;
QUINOLINE DERIVATIVE;
TRIFLUOROMETHANESULFONIC ACID METHYL ESTER;
UNCLASSIFIED DRUG;
ARTICLE;
ARYLATION;
CATALYSIS;
CATALYST;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
DRUG SYNTHESIS;
METHYLATION;
ONE POT SYNTHESIS;
PRIORITY JOURNAL;
|
EID: 78650512916
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2010.10.077 Document Type: Article |
Times cited : (26)
|
References (15)
|