Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Jiawei Rong"'
Autor:
Jiawei Rong, Juan F. Collados, Pablo Ortiz, Ravindra P. Jumde, Edwin Otten, Syuzanna R. Harutyunyan
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-7 (2016)
The stereoselective addition of Grignard reagents to ketimines is potentially a straightforward route to α-chiral amines. Here the authors report a catalytic, asymmetric Grignard addition to silyl ketimines, givingN-sulfonyl protected α-chiral sily
Externí odkaz:
https://doaj.org/article/21be2c4928f94b7f9adb7908f0ebc4c3
Publikováno v:
International Journal of Wireless Information Networks. 29:1-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f09f061984c51a6016be2af8af5c29d
https://doi.org/10.1007/s10776-021-00540-9
https://doi.org/10.1007/s10776-021-00540-9
Publikováno v:
Experimental and Therapeutic Medicine. 14:1227-1234
MicroRNA-92a (miR-92a) was recently reported to have an oncogenic role in cervical cancer; however, the underlying mechanism remains largely unclear. The present study aimed to investigate the expression, clinical significance and regulatory mechanis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d37178a7343ac414ff316f9118f016bf
https://doi.org/10.3892/etm.2017.4586
https://doi.org/10.3892/etm.2017.4586
Publikováno v:
Computers & Chemical Engineering. 133:106638
In this study, a model order reduction (MOR) technique is proposed to address the challenges of controlling large-scale problems for model predictive control (MPC) development in continuous chemical processing to meet the real-time control requiremen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5a805691837bfa05cfbed82df2b26a2
https://doi.org/10.1016/j.compchemeng.2019.106638
https://doi.org/10.1016/j.compchemeng.2019.106638
Publikováno v:
Human pathology. 85
Collagen triple helix repeat containing 1 (CTHRC1) is overexpressed in different kinds of cancer tissues and may thus promote tumor formation. Thus, we aimed to explore whether CTHRC1 could be a predictor of clinical significance including survival i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90217d5c3c4137dc8db125d0a788dad
https://pubmed.ncbi.nlm.nih.gov/30381261
https://pubmed.ncbi.nlm.nih.gov/30381261
Publikováno v:
Organic letters. 20(13)
Unprotected α-amino carbon radicals are produced as novel intermediates via a transformation that merges acid-promoted N–H imine generation and chemoselective photocatalytic single-electron reduction. Coupling ammonia and aldehydes/ketones allows
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c1ca6d1a451f1c3de496c217dac4d7a
https://pubmed.ncbi.nlm.nih.gov/29947523
https://pubmed.ncbi.nlm.nih.gov/29947523
Publikováno v:
Catalysis Science & Technology, 4(7), 1997-2005. ROYAL SOC CHEMISTRY
A series of new copper complexes containing chiral ferrocenyl diphosphine ligands of the Josiphos family have been prepared. These complexes have been studied in the catalytic asymmetric 1,2-addition of Grignard reagents to enones and aromatic ketone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::059d67284c567bbae6b469b4a4ed7fbf
https://doi.org/10.1039/c4cy00180j
https://doi.org/10.1039/c4cy00180j
Autor:
Edwin Otten, Jiawei Rong, Syuzanna R. Harutyunyan, Juan F. Collados, Pablo Ortiz, Ravindra P. Jumde
Publikováno v:
Nature Communications
Nature Communications, 7:13780. Nature Publishing Group
Nature Communications, Vol 7, Iss 1, Pp 1-7 (2016)
Nature Communications, 7:13780. Nature Publishing Group
Nature Communications, Vol 7, Iss 1, Pp 1-7 (2016)
α-Chiral amines are of significant importance in medicinal chemistry, asymmetric synthesis and material science, but methods for their efficient synthesis are scarce. In particular, the synthesis of α-chiral amines with the challenging tetrasubstit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::786357f35a6826678c35f97eb7b28124
https://pubmed.ncbi.nlm.nih.gov/28008909
https://pubmed.ncbi.nlm.nih.gov/28008909
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13022c2e4a577749b46a320fec136641
https://doi.org/10.1002/chin.201620234
https://doi.org/10.1002/chin.201620234
Publikováno v:
ChemInform. 46
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by a copper diphosphine complex.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf823a4c6dfbbb1fba59ee40ae787cb3
https://doi.org/10.1002/chin.201528242
https://doi.org/10.1002/chin.201528242