Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Aiichiro Ori"'
Publikováno v:
Chemistry Letters. 25:301-302
A calix[4]arene bearing three amide groups (composing a lanthanide binding site) and one sensitizer (phenacyl group) bearing an (o-boronylphenyl)methylaminomethyl group (acting as a sugar-binding site) was synthesized. The energy-transfer to Eu3+ was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1f8d2d42cbcd6642ffc2094d3936324
https://doi.org/10.1246/cl.1996.301
https://doi.org/10.1246/cl.1996.301
Publikováno v:
Chemical Communications. :407
F– and saccharides which feature specific affinity with the bornic acid group can be detected visually by the redox reaction between ferrocenylboronic acid derivatives and dyes with the appropriate redox potentials.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::020b945c17a91478b17e74ad01cc244c
https://doi.org/10.1039/cc9960000407
https://doi.org/10.1039/cc9960000407
Autor:
Seiji Shinkai, Aiichiro Ori
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1771
A chiral ferrocenylboronic acid 1 bearing an intramolecular tertiary amine binds saccharides at ca. pH 7, the complexation event, which can be conveniently detected by an electrochemical method, shows chiral discrimination for certain linear sacchari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b918c8998539dea6620c12c2af95c8ff
https://doi.org/10.1039/c39950001771
https://doi.org/10.1039/c39950001771
Publikováno v:
Chemistry Letters. 15:13-16
Hydrolysis of optically pure 1-alkenyl-2-sulfonyloxy-1-propanone acetals afforded optically and geometrically pure title compounds via stereospecific 1,2-rearrangement of alkenyl group.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ae40f6b68c96d2baba0e5c095f21c07
https://doi.org/10.1246/cl.1986.13
https://doi.org/10.1246/cl.1986.13
Publikováno v:
Chemistry Letters. 16:1259-1262
Chiral sesquiterpenes, (+)-Davanone and (+)-Artemone, were synthesized via anti-selective epoxidation and iodo-cyclization by the use of (S)-ethyl lactate as a chiral source.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c53881798d56545e8fe701d7068fbfd
https://doi.org/10.1246/cl.1987.1259
https://doi.org/10.1246/cl.1987.1259
Publikováno v:
Bulletin of the Chemical Society of Japan. 60:1027-1036
(S)-1-Aryl-2-sulfonyloxy-1-alkanone acetals, prepared from natural ethyl (S)-lactate or (S)-valine (chiral sources) by the use of a Grignard reaction, were rearranged under hydrolytic conditions in the presence of a base to give (S)-2-arylalkanoic es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e912789ee5c25048a34b67b5923b011
https://doi.org/10.1246/bcsj.60.1027
https://doi.org/10.1246/bcsj.60.1027
Publikováno v:
Chemischer Informationsdienst. 17
Hydrolysis of optically pure 1-alkenyl-2-sulfonyloxy-1-propanone acetals afforded optically and geometrically pure title compounds via stereospecific 1,2-rearrangement of alkenyl group.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16b519f57bee413b7ffbba4607da7948
https://doi.org/10.1002/chin.198646191
https://doi.org/10.1002/chin.198646191
Publikováno v:
ChemInform. 18
Title compounds were treated with EtAlCl2 or TiC3OPri and t-butyl hydroperoxide (TBHP) at −78 °C, followed by K2CO3 to give anti-epoxide, which reacted with LiAlH4 at γ-position.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::699db049d2fbc55fe8f4211ae58f662c
https://doi.org/10.1002/chin.198709153
https://doi.org/10.1002/chin.198709153
Publikováno v:
ChemInform. 18
(S)-1-Aryl-2-sulfonyloxy-1-alkanone acetals, prepared from natural ethyl (S)-lactate or (S)-valine (chiral sources) by the use of a Grignard reaction, were rearranged under hydrolytic conditions in the presence of a base to give (S)-2-arylalkanoic es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14e78fde3d5bc521ef2e9e89c024f904
https://doi.org/10.1002/chin.198732159
https://doi.org/10.1002/chin.198732159