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pro vyhledávání: '"Nana Yoshino"'
Publikováno v:
Organic letters.
The first diastereoselective synthesis of trisubstituted cubanes was achieved using a chiral auxiliary. To establish chirality within the cubane skeleton, at least three substituents must be introduced at the appropriate positions. Ready conversion o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4857291ec626987988011d7f79666b5
https://pubmed.ncbi.nlm.nih.gov/36594869
https://pubmed.ncbi.nlm.nih.gov/36594869
Publikováno v:
Israel Journal of Chemistry. 61:380-386
Cubane, a hexahedral hydrocarbon, can be converted into an asymmetric molecule with a minimum of three substituents. The resulting chiral cubane can be used as a pharmacophore or a chiral ligand. Starting from the cubane carboxamide, the 1,2,3-substi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96ccc9ac38aec01ff9d927bb66349a8f
https://doi.org/10.1002/ijch.202100013
https://doi.org/10.1002/ijch.202100013
Autor:
Yumi Kato, Mei Harada, Seijiro Matsubara, Masanobu Uchiyama, Nana Yoshino, Atsuya Muranaka, Thibaud Mabit, Yuuya Nagata, Craig M. Williams
Publikováno v:
Organic Letters. 22:4083-4087
In the hexahedral hydrocarbon cubane, replacing hydrogen with other atoms at three positions within any one of the internal tetrahedrons can conceptually lead to the formation of a unique class of chiral molecules. In pursuit of this endeavor, we pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18bf82ee47bf4106811c5672280cb45a
https://doi.org/10.1021/acs.orglett.0c01142
https://doi.org/10.1021/acs.orglett.0c01142
Publikováno v:
HETEROCYCLES. 103:769
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee0c65c768b2d14dac8d98381dca00b8
https://doi.org/10.3987/com-20-s(k)36
https://doi.org/10.3987/com-20-s(k)36