ANNULATION REACTION;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL ANALYSIS;
CHEMICAL STRUCTURE;
ETHERIFICATION;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
ROOM TEMPERATURE;
SONOGASHIRA REACTION;
SYNTHESIS;
X RAY ANALYSIS;
When the coupling reaction leading to 6a was carried out by using 20 mol% of the catalyst and 20 equiv. of 1,2-diiodobenzene, the product yield was improved to 59%.
When the coupling reaction leading to 6a was carried out by using 20 mol% of the catalyst and 20 equiv. of 1,2-diiodobenzene, the product yield was improved to 59%.
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For example, 86% of 1,2-diiodobenzene was recovered in the reaction of 5a.
For example, 86% of 1,2-diiodobenzene was recovered in the reaction of 5a.
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Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC Number: 213427. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK [fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac. uk].
Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC Number: 213427. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK [fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac. uk].
* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.