Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Hiraku Ishihara"'
Publikováno v:
ChemInform. 21
Reactions des sels de sodium de tosylhydrazones de thiophene-2- et -3-carbaldehydes, de furfural et de 1-methyl pyrrole-2-carbaldehyde (A) avec l'ethynylbenzene; obtention des 3-heteryl-5-phenylpyrazoles correspondants et, dans le cas de A, de 1,1'-d
Publikováno v:
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry. 73:309-312
1. The circulating erythrocytes of Rana catesbeiana tadpoles at varying metamorphic stages were studied by the phthalate-microcapillary technique of Danon & Marikovsky (1964 J. Lab. Clin. Med. 64, 668-674) and by the method of Murphy (1973 J. Lab. Cl
Autor:
Hiraku Ishihara
Publikováno v:
Journal of Nippon Medical School. 46:393-403
Autor:
Hiraku Ishihara, Katsuhiro Saito
Publikováno v:
Bulletin of the Chemical Society of Japan. 59:1095-1098
The rearrangement of the carbene, cycloheptatrienylidene, to the allene, 1,2,4,6-cycloheptatetraene, was investigated. Tropone tosylhydrazone sodium salt, the precursor of cycloheptatrienylidene was decomposed in the presence of various kinds of 9-su
Publikováno v:
Bulletin of the Chemical Society of Japan. 60:4317-4320
The addition reactions of 2-thienylmethylene with cis- and trans-stilbene afforded stereospecific adducts, respectively, indicating that the multiplicity of the carbene is singlet. The nucleophilicity of the carbenes was elucidated by an investigatio
Publikováno v:
Bulletin of the Chemical Society of Japan. 62:1925-1929
Reactions of the sodium salts of tosylhydrazones of several heteroaromatic aldehydes with an equimolar amount of acrylonitrile afforded the corresponding cyclopropane derivatives as the major products accompanied by small amounts of pyrazole derivati
Autor:
Katsuhiro Saito, Hiraku Ishihara
Publikováno v:
Bulletin of the Chemical Society of Japan. 58:2664-2668
Tropone tosylhydrazone sodium salt, the precursor of the cyclic conjugated carbene (cycloheptatrienylidene), was decomposed in the presence of various cyclopentadienone derivatives to give endo- and exo-[4+2]-type adducts and benzotropylidene derivat
Autor:
Hiraku Ishihara, Katsuhiro Saito
Publikováno v:
Chemischer Informationsdienst. 17
Publikováno v:
Bulletin of the Chemical Society of Japan. 60:4141-4142
Reactions of benzocyclopropene with furan and benzofuran afforded [2π+2σ]-type cycloaddition products, where the furans act as 2π-components and benzocyclopropene acts as a 2σ-component. A similar reaction with 1,3-diphenylisobenzofuran gave a [4
Autor:
Katsuhiro Saito, Hiraku Ishihara
Publikováno v:
Bulletin of the Chemical Society of Japan. 60:4447-4448
The reaction of tropone tosylhydrazone sodium salt with 3- or 5-methoxycarbonyl-2-pyrones afforded benzotropilidene derivatives. These products are considered to be formed via addition reactions of the 2-pyrone derivatives with 1,2,4,6-cycloheptatetr