Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Seiko Nan'ya"'
Publikováno v:
Journal of Heterocyclic Chemistry. 32:1299-1302
o-Monobromoacetylacylphenones, 3a and 3b reacted with hydroxylamine or hydrazine hydrate to produce heterocycles, 2,3-benzoxazine or phthalazine derivatives. The reaction of bromoacetyl group of 3a and 3b with several thioamides afforded thiazole der
Publikováno v:
ChemInform. 23
Double 1,3-dipolar cycloadditions of 2,4-diphenyl-3-methyloxazotium 5-oxide and 3-phenylsydnone to two molecules of N-substituted maleimide afforded one or two isomeric 4,8-iminobenzo[1,2-c:4,5-c′]dipyrrole-1,3,5,7-tetrone derivatives owing to the
Publikováno v:
ChemInform. 23
The reactions of o-diacylbenzenes with primary amines or ammonia produced several isoindole derivatives in the presence or the absence of acid. From o-diacylbenzenes and hydroxylamine hydrochloride in the presence of triethylamine 1H-2,3-benzoxazine
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 24
2-Bromoinden-1-ones 2 were condensed with 6-substituted 3-aminopyridine-2(1H)-thiones to produce a new type of 4-azaindeno[2,1-b][1,4]benzothiazine derivatives 3. Substituted 6-phenylindeno[2,1-b][1,4]benzothiazines 4 were also prepared by reacting 2
Publikováno v:
ChemInform. 24
2-Bromo-3-substituted-inden-1-ones 2 reacted with L-cysteine or 2-aminobenzenethiol to produce 2,3-dihydro-5-phenylindeno[2,1-b][1,4]thiazine in moderate yield or 6-substituted-indeno[2,1-b][1,4]benzothiazines in good yield. The debrominated oxime an
Publikováno v:
ChemInform. 26
2-Bromo-3-phenylinden-1-one (2) reacted with phenylthiourea to produce 2-phenylimino-8-phenylindeno[1,2-d]thiazole (heteropentalene) (4) in moderate yield and bis-substituted-indenyl sulfide (5) in low yield. Whereas, from the reaction of (2) with th
Publikováno v:
ChemInform. 26
o-Dibromoacetylbenzophenone, 2 or o-bromoacetylbenzophenone 3 reacted with aqueous ammonia to produce 3-phenylisoindolin-1-one 5. The reaction of 3 with methylamine afforded 3-hydroxy-2-methyl-3-phenyl-isoindolin-1-one 4 and 2-methyl-3-phenylisoindol
Publikováno v:
ChemInform. 26
o-Monobromoacetylacylphenones, 3a and 3b reacted with hydroxylamine or hydrazine hydrate to produce heterocycles, 2,3-benzoxazine or phthalazine derivatives. The reaction of bromoacetyl group of 3a and 3b with several thioamides afforded thiazole der
Publikováno v:
Journal of Heterocyclic Chemistry. 29:1525-1528
2-Bromo-3-substituted-inden-1-ones 2 reacted with L-cysteine or 2-aminobenzenethiol to produce 2,3-dihydro-5-phenylindeno[2,1-b][1,4]thiazine in moderate yield or 6-substituted-indeno[2,1-b][1,4]benzothiazines in good yield. The debrominated oxime an