Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Ya Mei Lin"'
Autor:
Guan-Lin Chen, Shang-Yi Lin, Hsiang-Yi Lo, Hsaing-Chun Wu, Ya-Mei Lin, Tun-Chieh Chen, Chieh-Yu Sandy Chu, Wen-Chi Lee, Yen-Hsu Chen, Po-Liang Lu
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 54, Iss 5, Pp 952-962 (2021)
Background: It is unclear about the impact of recreational drug use on the adherence, drug–drug interaction and the occurrence of sexual transmitted diseases (STDs) among people living with HIV. Material and methods: A retrospective study was condu
Externí odkaz:
https://doaj.org/article/c556ec3bfc7f494caebed852926d0740
Autor:
Tun-Chieh Chen, Ya-Mei Lin, Wen-Chi Lee, Chieh-Yu Sandy Chu, Shang-Yi Lin, Yen-Hsu Chen, Hsaing-Chun Wu, Guan-Lin Chen, Hsiang-Yi Lo, Po-Liang Lu
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 54, Iss 5, Pp 952-962 (2021)
Background It is unclear about the impact of recreational drug use on the adherence, drug–drug interaction and the occurrence of sexual transmitted diseases (STDs) among people living with HIV. Material and methods A retrospective study was conduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3ce961834f09cf7be3d5fcb43af08f1
https://doi.org/10.1016/j.jmii.2020.07.016
https://doi.org/10.1016/j.jmii.2020.07.016
Publikováno v:
Asian Journal of Organic Chemistry. 8:627-636
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c70dbf9124a75666a02c029bc26015d2
https://doi.org/10.1002/ajoc.201900075
https://doi.org/10.1002/ajoc.201900075
Publikováno v:
Organic Letters. 19:1100-1103
A radical-mediated approach has been introduced for the C-S bond activation of arylalkenyl sulfides. The protocol provides an efficient approach for the generation of various alkenes including alkenyl silanes, sulfones, phosphine oxides, and nitroole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e2d736496f6e532f4cf5a785d365080
https://doi.org/10.1021/acs.orglett.7b00126
https://doi.org/10.1021/acs.orglett.7b00126
Publikováno v:
Advanced Synthesis & Catalysis. 358:4100-4105
Regioselective arylthiolations of aromatic amines, arenols and ketones via C–H bond functionalization have been achieved with I2 and PPh3 in an aqueous system, whereby arylsulfenyl radicals are in situ generated from odorless sodium arylsulfinates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9778c1083883a5af7cfe36a79bf058b
https://doi.org/10.1002/adsc.201600846
https://doi.org/10.1002/adsc.201600846
Publikováno v:
RSC Advances. 5:27107-27111
A newly developed C–S bond formation process via acid-catalyzed thia-Michael addition has been demonstrated. The protocol, in which Bunte salts generated from odorless and inexpensive sodium thiosulfate and organic halides are used as the thiol pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34be52f239beb3aaf786340698bfad84
https://doi.org/10.1039/c5ra01381j
https://doi.org/10.1039/c5ra01381j
Autor:
Ya-mei Lin, Guo-ping Lu
Publikováno v:
Journal of Chemical Research. 38:371-374
A novel base-catalysed 1,3,4-oxadiazole fragmentation for the synthesis of nitriles at room temperature has been developed. This reaction is performed under transition-metal-free conditions, and pr...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0977a19bff92e47f7558d37537528294
https://doi.org/10.3184/174751914x14007780679741
https://doi.org/10.3184/174751914x14007780679741
Publikováno v:
Organic letters. 18(24)
Transition-metal-free radical access to 1,4-benzothiazine derivatives from o-aminobenzenethiols is disclosed. This procedure is available for various ketones including α,β-unsaturated, cyclic, linear, and fluoroalkyl ketones to generate a number of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec85c7b4f62a7b5008b2dbaad9d55e93
https://pubmed.ncbi.nlm.nih.gov/27978628
https://pubmed.ncbi.nlm.nih.gov/27978628
Publikováno v:
The Journal of organic chemistry. 82(1)
A newly developed aqueous system with acid and phosphide was introduced in which odorless and stable sodium arylsulfinates can in situ generate arylsulfenyl radicals. These radicals have high reactivity to react with alkynes, alkenes, and H-phosphine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b1c8f29905f98304256e2bf0b228496
https://pubmed.ncbi.nlm.nih.gov/27936696
https://pubmed.ncbi.nlm.nih.gov/27936696
Publikováno v:
ChemInform. 47
α,α-Difluorodiaroylmethane can be used as a nucleophilic difluoromethylation reagent for generating α-thioaryl-α,α-difluoroacetophenones (Ar1COCF2SAr) and difluoromethylthiolated arenes (ArSCF2H) under transition-metal-free conditions. The react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::161f2458cd9e560569473bb131465d7d
https://doi.org/10.1002/chin.201626108
https://doi.org/10.1002/chin.201626108