Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Shizunobu Hashimoto"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20cdff277303e7f6a57603570c808c96
https://doi.org/10.1002/chin.199135125
https://doi.org/10.1002/chin.199135125
Publikováno v:
ChemInform. 22
ジハロトリフェニルポスホランと1-アリ-ル-2-ヒドロキシ-1-アルカノンジメチルアセタール1のi 反応について検討した。ジブモトリフェニルボスホラン2またはジグロロートリフェニルホス
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9100c06ea9c44685d26e6c14903173c
https://doi.org/10.1002/chin.199137124
https://doi.org/10.1002/chin.199137124
Publikováno v:
Journal of Inclusion Phenomena and Molecular Recognition in Chemistry. 13:287-293
Fluorescence spectroscopy has been used to determine the binding constants (K) for inclusion complexes of six kinds ofp-Akyphenols withβ-cyclodextrin (β-CDx), heptakis(2,6-di-O-methyl)-β-CDx (DMe-β-CDxg), and heptakis(2,3,6-tri-O-methyl)-β-CDx (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::342ec0e0fe2d7587422c3998d7a64dfe
https://doi.org/10.1007/bf01042787
https://doi.org/10.1007/bf01042787
Publikováno v:
The Journal of Organic Chemistry. 56:6579-6585
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7ee83da7e5a7e170f1bdce7932632b3
https://doi.org/10.1021/jo00023a024
https://doi.org/10.1021/jo00023a024
Publikováno v:
The Journal of Physical Chemistry. 95:7839-7843
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::246503f39fc3f680af42a29c726e093e
https://doi.org/10.1021/j100173a052
https://doi.org/10.1021/j100173a052
Publikováno v:
Journal of Macromolecular Science: Part A - Chemistry. 28:475-486
The synthesis of a linear polymer having a tertiary amino group in a part of the main chain has been attempted by several methods. However, it was difficult for the linear polyamine to form because of the complicated reaction of the amino group. In t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba1eb91761ffc427842014cd8002ab87
https://doi.org/10.1080/00222339108052101
https://doi.org/10.1080/00222339108052101
Publikováno v:
Bulletin of the Chemical Society of Japan. 64:778-784
The stability of the molecular complexes between 5,10,15,20-tetraarylporphyrins and quinones in organic solvents has been compared with that in water. 5,10,15,20-Tetrakis(mono-substituted phenyl)porphines (RTPPs) hardly form molecular complexes with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd37c10f079763a1585d625b34d4db86
https://doi.org/10.1246/bcsj.64.778
https://doi.org/10.1246/bcsj.64.778
Publikováno v:
The Journal of Physical Chemistry. 95:966-970
Les interactions entre le desoxycholate de sodium (molecule hote) et ses analogues insolubles dans l'eau (molecule invitee) sont etudiees dans l'eau a pH=10 afin de determiner les mecanismes de formation des premicelles et des micelles de desoxychola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfd4cfa3e12958ba0463fb62e29f6948
https://doi.org/10.1021/j100155a086
https://doi.org/10.1021/j100155a086
Publikováno v:
Chemistry Letters. 19:1381-1384
Hemin promotes the Markovnikov-type addition reactions of thiols (origins of the thiols are their disulfide derivatives) to styrene in benzene–ethanol (1:1) containing NaBH4. The plausible reaction mechanism has been discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e934eb64af50d39a2e8962d0665731e0
https://doi.org/10.1246/cl.1990.1381
https://doi.org/10.1246/cl.1990.1381
Publikováno v:
The Journal of Physical Chemistry. 94:2181-2187
Three kinds of cationic porphyrins have been employed to study intermolecular interaction of these porphyrins in water. Fluorescence behavior of 4,4',4'',4'''-(21H,23H-porphine-5,10,15,20-tetrayl) tetrakis [1-octylpyridinium] tetrachloride (TOPyP) is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::541f5324d4e5f585c060dbfbc2163795
https://doi.org/10.1021/j100368a082
https://doi.org/10.1021/j100368a082