Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Pei-Xin Rui"'
Publikováno v:
Organic Letters; 7/26/2024, Vol. 26 Issue 29, p6225-6229, 5p
Publikováno v:
In Physics and Chemistry of the Earth February 2020 115
Publikováno v:
Organicbiomolecular chemistry. 20(27)
We have developed an improved cyanide-free strategy for the synthesis of glycosyl carboxylic acids, employing stereoselective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1807e6f9ef1caf4848eca8061c252d66
https://pubmed.ncbi.nlm.nih.gov/35770913
https://pubmed.ncbi.nlm.nih.gov/35770913
Publikováno v:
European Journal of Organic Chemistry. 2019:1715-1721
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55b35223bfa4a59b6129090a952ed8ed
https://doi.org/10.1002/ejoc.201801334
https://doi.org/10.1002/ejoc.201801334
Publikováno v:
Organicbiomolecular chemistry. 17(45)
We have realized the first Ullmann type coupling reaction of tri(di)fluoroethylamine with (hetero)aromatic bromides, employing 5–20 mol% Cu2O and an oxalamide ligand [N-(2,4,6-trimethoxyphenyl)acetamide]. This efficient and practical method has the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af9815109bcbb7530a9dd6764dd90a60
https://pubmed.ncbi.nlm.nih.gov/31709436
https://pubmed.ncbi.nlm.nih.gov/31709436
Publikováno v:
Organicbiomolecular chemistry. 16(47)
The transformation of hydroximoyl fluorides to nitrile oxides for [3 + 2]-cycloaddition with alkynes has been achieved for the first time. The hydroximoyl fluorides used in this work appeared to be not stable, which was proved by a series of experime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d31a35d9a8d59eaf005da8cdf5a550
https://pubmed.ncbi.nlm.nih.gov/30468229
https://pubmed.ncbi.nlm.nih.gov/30468229
Publikováno v:
European Journal of Organic Chemistry. 2019:1685-1685
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59d7980c99c6ed410b625ec514125cd0
https://doi.org/10.1002/ejoc.201900227
https://doi.org/10.1002/ejoc.201900227
Autor:
Pei-Xin Rui, Xin Chen, Yue-Mei Jia, Xihui He, Ruirui He, Junfeng Xiang, Jia-Kun Su, Nanyin Han, Chu-Yi Yu, Jinghua Zhu
Publikováno v:
Synlett. 2010:1609-1616
Friedel-Crafts-type reaction of electron-rich aromatic compounds with polyhydroxylated cyclic nitrones catalyzed by Bronsted acid afforded 2-aryl polyhydroxylated pyrrolidines in good to excellent yields with high diastereoselectivity under mild cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41ce894e96e2ab5d7ba789692db02e38
https://doi.org/10.1055/s-0029-1258085
https://doi.org/10.1055/s-0029-1258085
Autor:
Chu-Yi Yu, Jia-Kun Su, Pei-Xin Rui, Jinghua Zhu, Xihui He, Ruirui He, Xin Chen, Yue-Mei Jia, Nanyin Han, Junfeng Xiang
Publikováno v:
ChemInform. 41
Nitrones (I), (XI) and (XV) undergo Friedel—Crafts-type reaction with electron-rich aromatic compounds in the presence of HCl, generated in situ, to produce the corresponding iminosugar with generally high diastereoselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e7276a7fb072a2c46be83d317f88bf4
https://doi.org/10.1002/chin.201046185
https://doi.org/10.1002/chin.201046185