Pub. Date : 2000 Apr 6
PMID : 10768195
3 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | A concise synthetic route to physostigmine has been developed, where the key step relies on the alkylative cyclization of 1,3-dimethylindole with (Z)-aziridine catalyzed by Sc(OTf)3 and TMSCI in dichloromethane at -30 degrees C, to give 8 in 90% yield, which, in turn, can be readily converted into physostigmine. | Physostigmine | POU class 5 homeobox 1 | Homo sapiens |
2 | A concise synthetic route to physostigmine has been developed, where the key step relies on the alkylative cyclization of 1,3-dimethylindole with (Z)-aziridine catalyzed by Sc(OTf)3 and TMSCI in dichloromethane at -30 degrees C, to give 8 in 90% yield, which, in turn, can be readily converted into physostigmine. | 1,3-Dimethylindole | POU class 5 homeobox 1 | Homo sapiens |
3 | A concise synthetic route to physostigmine has been developed, where the key step relies on the alkylative cyclization of 1,3-dimethylindole with (Z)-aziridine catalyzed by Sc(OTf)3 and TMSCI in dichloromethane at -30 degrees C, to give 8 in 90% yield, which, in turn, can be readily converted into physostigmine. | (z)-aziridine | POU class 5 homeobox 1 | Homo sapiens |