Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Taro Sonehara"'
Publikováno v:
Tetrahedron Letters. 60:598-601
We investigated the palladium-catalyzed [2 + 2 + 1] cycloaddition of aryl- and trifluoromethyl-group-substituted internal alkynes and carbon monoxide, and revealed that the PdBr2 effectively catalyzed the intended reaction. The PdBr2-catalyzed reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::567953c4093e179f4d83250833613961
https://doi.org/10.1016/j.tetlet.2019.01.036
https://doi.org/10.1016/j.tetlet.2019.01.036
Publikováno v:
Synlett. 27:2029-2033
We demonstrated the intermolecular [2+2+2] cycloaddition of aryl- and trifluoromethyl-substituted internal alkyne and ethyl cyanoformate, and succeeded in constructing the pyridine derivatives using the CoI2/dcype/Zn catalyst system. The reaction p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f6b81a416c02e8387e833324f1a62fb
https://doi.org/10.1055/s-0035-1562432
https://doi.org/10.1055/s-0035-1562432
Publikováno v:
Organic letters. 19(16)
We demonstrate the iron-catalyzed intermolecular coupling of internal alkynes and thiosalicylic acid derivatives. The reaction was effectively catalyzed by the Fe(acac)2/1,10-phenanthroline catalyst in toluene/HFIP (hexafluoroisopropyl alcohol) as th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f957d139649d20df4e27ca92b60093ef
https://pubmed.ncbi.nlm.nih.gov/28783361
https://pubmed.ncbi.nlm.nih.gov/28783361
Publikováno v:
ChemInform. 47
We demonstrated the intermolecular [2+2+2] cycloaddition of aryl- and trifluoromethyl-substituted internal alkyne and ethyl cyanoformate, and succeeded in constructing the pyridine derivatives using the CoI2/dcype/Zn catalyst system. The reaction p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2bd935a410514013735a0a94c3a9ef3
https://doi.org/10.1002/chin.201652299
https://doi.org/10.1002/chin.201652299
Publikováno v:
ChemInform. 47
The copper-catalyzed regioselective intermolecular hydroamination of the aryl and trifluoromethyl group or electron-withdrawing group substituted internal alkynes with amines has been accomplished. The reaction was effectively catalyzed by the ligand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdbe4f8432f4318b889b09f4f635ade8
https://doi.org/10.1002/chin.201630085
https://doi.org/10.1002/chin.201630085
Publikováno v:
Organic letters. 18(6)
The copper-catalyzed regioselective intermolecular hydroamination of the aryl and trifluoromethyl group or electron-withdrawing group substituted internal alkynes with amines has been accomplished. The reaction was effectively catalyzed by the ligand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dccdee469835c656e7c680a96d37639
https://pubmed.ncbi.nlm.nih.gov/26954725
https://pubmed.ncbi.nlm.nih.gov/26954725
Publikováno v:
Organic Letters; Aug2017, Vol. 19 Issue 16, p4299-4302, 4p
Publikováno v:
Synlett; 2016, Vol. 27 Issue 13, p2029-2033, 5p
Publikováno v:
Organic Letters; Mar2016, Vol. 18 Issue 6, p1422-1425, 4p