Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kenji Kukita"'
Autor:
Miki Kawada-Matsuo, Yasuo Suda, Hitoshi Komatsuzawa, Mami Nagatomo, Kenji Kukita, Takahiko Oho, Masahito Hashimoto, Yuichi Oogai, Takuo Tanaka
Publikováno v:
Infection and Immunity. 81:1870-1879
Staphylococcus aureus is a major human pathogen that can colonize the nasal cavity, skin, intestine, and oral cavity as a commensal bacterium. gp340, also known as DMBT1 (deleted in malignant brain tumors 1), is associated with epithelial differentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a78869758cafc3a0f476dd41193d744f
https://doi.org/10.1128/iai.00011-13
https://doi.org/10.1128/iai.00011-13
Autor:
Kazuki Osakama, Kenji Kukita, Makoto Nakajima, Midori Sakamoto, Rika Watanabe, Daijiro Takemoto
Publikováno v:
HETEROCYCLES. 97:708
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dddd1f6a2a32cbd27c346518f833f5c
https://doi.org/10.3987/com-18-s(t)63
https://doi.org/10.3987/com-18-s(t)63
Publikováno v:
Chemical Communications. 47:5614-5616
Chiral lithium binaphtholate effectively catalyzed the enantioselective alkynylation of ketones using lithium acetylide as an alkynylating agent. This is the first example of the catalytic enantioselective addition of lithium acetylide to carbonyl co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4663b51b1f02648f71a0ed4e566adae1
https://doi.org/10.1039/c1cc10734h
https://doi.org/10.1039/c1cc10734h
Publikováno v:
ChemInform. 45
Best results in the reactions with ketones are obtained by adding a solution of the ketone to the acetylide over a period of one hour.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cce29be756d050e898fcb4df468f28f1
https://doi.org/10.1002/chin.201447027
https://doi.org/10.1002/chin.201447027
Publikováno v:
The Journal of organic chemistry. 79(11)
The asymmetric addition of lithium acetylides to carbonyl compounds in the presence of a chiral lithium binaphtholate catalyst was developed. A procedure involving the slow addition of carbonyl compounds to lithium acetylides improved the enantiosele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15054fe78cf7edb13108fbcf1bbea1fc
https://pubmed.ncbi.nlm.nih.gov/24750104
https://pubmed.ncbi.nlm.nih.gov/24750104
Publikováno v:
ChemInform. 42
Optically active propargyl alcohols are synthesized via the enantioselective addition of lithium acetylides to ketones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5348f3caa537394ded4a6a1a9c84c4e7
https://doi.org/10.1002/chin.201137029
https://doi.org/10.1002/chin.201137029
Publikováno v:
Journal of Organic Chemistry; 6/6/2014, Vol. 79 Issue 11, p4817-4825, 9p