Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Masanao Terashima"'
Autor:
Minoru Ishikura, Masanao Terashima
Publikováno v:
Journal of Heterocyclic Chemistry. 31:977-980
On the preferential formation of 3-substituted indoles from triethyl (1-methylindol-2-yl)borate in the presence of cuprous cyanide and cationic electrophiles, it was supposed that the reaction seems to proceed through a transposition path from boron
Autor:
Minoru Ishikura, Masanao Terashima
Publikováno v:
The Journal of Organic Chemistry. 59:2634-2637
Publikováno v:
Chemical and Pharmaceutical Bulletin. 41:1920-1924
Reactive entities in the photoreaction of 2-, 3- and 4-iodopyridines with substituted benzenes were investigated; 3- and 4-pyridylation could be explained in terms of radical reaction, while the 2-pyridyl cation was an important intermediate in the 2
Publikováno v:
ChemInform. 22
Autor:
Minoru Ishikura, Masanao Terashima
Publikováno v:
ChemInform. 22
The conjugate addition reaction of triethyl(1- methyl-indol-2-yl) borate to 2-cycloalkenone could be effected with a catalytic amount of vinyloxyborane
Publikováno v:
ChemInform. 23
Autor:
Masanao Terashima, Minoru Ishikura
Publikováno v:
ChemInform. 24
A novel one-pot procedure for [ a ]-annelated indole via cyclic trialkyl(indol-2-yl)borate is described.
Publikováno v:
ChemInform. 24
2-Aroyl-1H-indoles were directly obtained by the reaction of 1-(N-aroylcarbamoyl) indoles, prepared from 1-(2-oxazolinyl) indole and aroyl chlorides, with LDA
Publikováno v:
ChemInform. 25
The reactions of the sodium salts of indoles with 2- and 4-fluoropy- ridines afforded the corresponding N-pyridylindoles in good yields, whereas the reaction with 3-fluoropyridine gave no coupling product
Autor:
Masanao Terashima, Minoru Ishikura
Publikováno v:
ChemInform. 26
On the preferential formation of 3-substituted indoles from triethyl (1-methylindol-2-yl)borate in the presence of cuprous cyanide and cationic electrophiles, it was supposed that the reaction seems to proceed through a transposition path from boron