Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tsukushi Tanaka"'
Autor:
Taro Tsuji, Kayoko Hashiguchi, Mana Yoshida, Tetsu Ikeda, Yunosuke Koga, Yusaku Honda, Tsukushi Tanaka, Suyong Re, Kenji Mizuguchi, Daisuke Takahashi, Ryo Yazaki, Takashi Ohshima
Publikováno v:
Nature Synthesis. 1:304-312
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd1b0ac1bf3dbe3cb3c2d224ca9081de
https://doi.org/10.1038/s44160-022-00037-0
https://doi.org/10.1038/s44160-022-00037-0
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 79:417-426
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dd826cdf0c66b91153c7f2016f59f81
https://doi.org/10.5059/yukigoseikyokaishi.79.417
https://doi.org/10.5059/yukigoseikyokaishi.79.417
Publikováno v:
Organic Letters. 22:4164-4170
We developed a catalytic aerobic method to synthesize α,α-disubstituted α-amino acids through cross-dehydrogenative coupling of azlactones. Combining an iron catalyst with a bisoxazolidine ligand resulted in high catalytic performance, and cross-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f44daa0245ab7cb5557051ac007adb24
https://doi.org/10.1021/acs.orglett.0c01248
https://doi.org/10.1021/acs.orglett.0c01248
Publikováno v:
Journal of the American Chemical Society. 142(9)
We developed a chemoselective catalytic activation of carboxylic acid for a 1e- radical process. α-Oxidation of a variety of carboxylic acids, which preferentially undergo undesired decarboxylation under radical conditions, proceeded efficiently und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98ec1f0d8f49236ed6e3535f4ed2fe86
https://pubmed.ncbi.nlm.nih.gov/32052625
https://pubmed.ncbi.nlm.nih.gov/32052625
Publikováno v:
ACS Catalysis. 8:8430-8440
Chemoselective iron-catalyzed dehydrogenative cross-coupling using 2-acylimidazoles is described. The addition of a phosphine oxide ligand substantially facilitated the generation of tert-butoxy radicals from di-tert-butyl peroxide, allowing for effi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b93c0f74e161356ac23dcf9cc109c6
https://doi.org/10.1021/acscatal.8b02361
https://doi.org/10.1021/acscatal.8b02361
Publikováno v:
Organic letters. 20(12)
A new strategy, a transient homocoupling dimer strategy, for direct catalytic oxidative cross-enolate coupling reactions is developed. Cross-enolate coupling products bearing a (contiguous) tetrasubstituted carbon center were obtained chemoselectivel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de3e8cd8dd08fa103df0a407d585e71a
https://pubmed.ncbi.nlm.nih.gov/29851494
https://pubmed.ncbi.nlm.nih.gov/29851494