Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jared M. Lowe"'
Publikováno v:
The Journal of Organic Chemistry. 87:12065-12071
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f896ef5db8970f48dc8cc1aa787aa29
https://doi.org/10.1021/acs.joc.2c01151
https://doi.org/10.1021/acs.joc.2c01151
Publikováno v:
ACS Catal
We introduce an organocatalytic approach for oxaziridinium-mediated C–H hydroxylation that employs secondary amines as catalysts. We also demonstrate the advantages of this operationally simple catalytic strategy for achieving high yielding and hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::492a7866f361cdc2bb41f3f73f500b87
https://pubmed.ncbi.nlm.nih.gov/35529672
https://pubmed.ncbi.nlm.nih.gov/35529672
Autor:
Weijun Yu, Qisheng Gu, Di Wu, Weiqi Zhang, Gang Li, Lu Lin, Jared M. Lowe, Shucheng Hu, Tia Wenjun Li, Zhen Zhou, Michael Z. Miao, Yuhua Gong, Yifei Zhao, Eryi Lu
Publikováno v:
Journal of Periodontal Research. 57:594-614
Periodontitis is a multifactorial chronic inflammatory disease that can lead to the irreversible destruction of dental support tissues. As an epigenetic factor, the expression of circRNA is tissue-dependent and disease-dependent. This study aimed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05abb8e83a811454d7e09e84ccbb998e
https://doi.org/10.1111/jre.12989
https://doi.org/10.1111/jre.12989
Publikováno v:
ACS Catalysis. 12:4302-4309
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51fd9d4319ecb5af1d84ccdec8633f5b
https://doi.org/10.1021/acscatal.2c00392
https://doi.org/10.1021/acscatal.2c00392
Publikováno v:
The Journal of organic chemistry. 87(18)
The condensative cyclization of sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c6fc7a40ea320b3c52ca4c2032e67fb6
https://pubmed.ncbi.nlm.nih.gov/36053236
https://pubmed.ncbi.nlm.nih.gov/36053236
Publikováno v:
Organic Letters. 23:5636-5640
A variety of C-glycosides can be obtained from the fluoroarylborane (B(C6F5)3) or silylium (R3Si+) catalyzed functionalization of 1-MeO- and per-TMS-sugars with TMS-X reagents. A one-step functionalization with a change as simple as the addition orde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b0c8fdc21233473cedbcda2b0f143c3
https://doi.org/10.1021/acs.orglett.1c01713
https://doi.org/10.1021/acs.orglett.1c01713
Publikováno v:
Chemical Science
Described are the first examples of Lewis acid-promoted Diels–Alder reactions of vinylpyridines and other vinylazaarenes with unactivated dienes. Cyclohexyl-appended azaarenes constitute a class of substructures of rising prominence in drug discove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c8e13a62510911999ca959b46c66cc5
https://doi.org/10.1039/d1sc05095h
https://doi.org/10.1039/d1sc05095h
Publikováno v:
Organometallics. 39:1258-1268
The stoichiometric addition of aryl and alkyl nitriles to the silylpalladium cation [(PCy3)2Pd–SiMe2Et+][(C6F5)4B–] (1) resulted in the cleavage of the nitrile C–CN bond and the formation of palladium–aryl and palladium–alkyl cations. Low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc6ca0f2ba9cd4dd0e009e7fcd419b34
https://doi.org/10.1021/acs.organomet.0c00034
https://doi.org/10.1021/acs.organomet.0c00034
Publikováno v:
Organic letters. 23(15)
A variety of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::336eee6172f0891806e9290445aca57b
https://pubmed.ncbi.nlm.nih.gov/34259527
https://pubmed.ncbi.nlm.nih.gov/34259527
Publikováno v:
ACS Catalysis. 9:6648-6652
The feedstocks from biomass are defined and limited by nature, but through the choice of catalyst, one may change the deoxygenation outcome. We report divergent but selective deoxygenation of sugar...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43596af8ff21d9d1668378f167681b8b
https://doi.org/10.1021/acscatal.9b01578
https://doi.org/10.1021/acscatal.9b01578