Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Daisuke Aburano"'
Autor:
Yuichi Sakanishi, Jitendra P. Mata, Kenji Aramaki, Kyuhei Kitao, Daisuke Aburano, Tetsuya Maehara, Chikahiro Iwata
Publikováno v:
Physical Chemistry Chemical Physics. 19:23802-23808
Bicelles are generally formed by phospholipid-based systems and are useful for various applications, such as nanocarriers or membrane protein crystallization. The same disc-like assemblies, nonionic surfactant bicelles (NSBs), can also be formed usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::610da997bbbc479ab74aebe7f9c76b16
https://doi.org/10.1039/c7cp02585h
https://doi.org/10.1039/c7cp02585h
Autor:
Tetsuya Maehara, Kenji Aramaki, Daisuke Aburano, Yoshitomo Tsukijima, Yuichi Sakanishi, Kyuhei Kitao, Junya Yamada
Publikováno v:
Langmuir. 31:10664-10671
Vesicles with synthetic nonionic surfactants are called niosomes or NSVs, and these have been the focus of attention as an alternative to phospholipid liposomes as drug carriers. Especially it is demanded to discover novel niosomal systems with polyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12fff183ee0fb96f87a37ca4f2eaafae
https://doi.org/10.1021/acs.langmuir.5b02454
https://doi.org/10.1021/acs.langmuir.5b02454
Publikováno v:
The Journal of Organic Chemistry. 74:5590-5594
Treatment of 3-(2-ethynylphenyl)prop-2-ynyl benzenesulfinate with 2.5 mol % of [RhCl(CO)(2)](2) at 40 degrees C under an atmosphere of CO effected the successive 2,3-sigmatropic rearrangement and carbonylative [2 + 2 + 1] ring-closing reaction to aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::726fad62183de75105ead4415bff5a01
https://doi.org/10.1021/jo901141t
https://doi.org/10.1021/jo901141t
Publikováno v:
The Journal of Organic Chemistry. 70:6045-6052
A highly stereoselective method for constructing a (2E)-methoxymethylidene-1,6-dioxaspiro[4.5]decane skeleton has been developed on the basis of the palladium(II)-catalyzed ring-closing reaction of the 3,4-dioxygenated-9-hydroxy-1-nonyn-5-one derivat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8abd3b3306fba57d23413199e07aaa6d
https://doi.org/10.1021/jo050822k
https://doi.org/10.1021/jo050822k
Publikováno v:
ChemInform. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d602ff7d40f0da966d4b02d752e2e14
https://doi.org/10.1002/chin.200952204
https://doi.org/10.1002/chin.200952204
Publikováno v:
ChemInform. 39
Upon treatment with 30 mol % of Co2(CO)8 and 30 mol % of TMTU in toluene at 70 °C, benzene-bridged alkynecarbodiimides efficiently underwent a ring-closing reaction to give the pyrrolo[2,3-b]indol-...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14dcb673d30be7751758f18a48390184
https://doi.org/10.1002/chin.200802115
https://doi.org/10.1002/chin.200802115
Publikováno v:
The Journal of organic chemistry. 72(18)
Upon treatment with 30 mol % of Co2(CO)(8) and 30 mol % of TMTU in toluene at 70 degrees C, benzene-bridged alkynecarbodiimides efficiently underwent a ring-closing reaction to give the pyrrolo[2,3-b]indol-2-ones in good yields. These conditions coul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::831480fb349a4ccac89158260f9a1c7a
https://pubmed.ncbi.nlm.nih.gov/17691742
https://pubmed.ncbi.nlm.nih.gov/17691742
Autor:
Kenji Aramaki, Junya Yamada, Yoshitomo Tsukijima, Tetsuya Maehara, Daisuke Aburano, Yuichi Sakanishi, Kyuhei Kitao
Publikováno v:
Langmuir; Oct2015, Vol. 31 Issue 39, p10664-10671, 8p