Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Jian‐Nan Xiang"'
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7234cdca97275db60a733a709de4f12
https://doi.org/10.1002/ejoc.202200434
https://doi.org/10.1002/ejoc.202200434
Publikováno v:
Organic letters. 23(24)
Nickel-catalyzed arylcarbamoylation reactions of alkenes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0d8790d3409b3ab66666ef464c23639
https://pubmed.ncbi.nlm.nih.gov/34860537
https://pubmed.ncbi.nlm.nih.gov/34860537
Publikováno v:
Organic letters. 23(15)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47cdafc6ccd9cd2c1b93200368109321
https://pubmed.ncbi.nlm.nih.gov/23987104
https://pubmed.ncbi.nlm.nih.gov/23987104
Publikováno v:
New Journal of Chemistry. 39:3093-3097
A new method for the preparation of (E)-β-alkylstyrene derivatives has been developed via the addition of a benzyl or alkyl radical to β-nitrostyrenes using di-tert-butyl peroxide (DTBP) as the oxidant in the presence of Cu powder catalyst. The C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e83ceefdf2391520d066c5a1d43f8a2
https://doi.org/10.1039/c4nj02416h
https://doi.org/10.1039/c4nj02416h
Publikováno v:
Organic Letters. 15:4654-4657
A novel method for the preparation of alkyl aryl sulfides through direct oxidation thiolation of commercial ethers with diaryl disulfides using di-tert-butyl peroxide (DTBP) as the oxidant without a metal catalyst was established. The C(sp(3))-H bond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d967e8c3324526cd0d3deee915c77a
https://doi.org/10.1021/ol402281f
https://doi.org/10.1021/ol402281f
Publikováno v:
Synlett. 24:443-448
Cu(OAc)2-promoted TBHP oxidative coupling reaction of formamides with thiols successfully proceeded through direct C–H bond activation of formamides. The corresponding S-phenyl dialkyl thiocarbamate compounds were formed with high yield under solve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2680b8562ead90c3d01869c7989c223a
https://doi.org/10.1055/s-0032-1318188
https://doi.org/10.1055/s-0032-1318188
Autor:
Ping Tan, Jian Nan Xiang
Publikováno v:
Advanced Materials Research. :970-974
Azetidin-3-ones are important heterocycles in organic synthesis and pharmaceutical chemistry. With gold-catalyzed alkyne intermolecular oxidation, these versatile heterocycles can be prepared in three steps from readily available propargylic alcohols
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fb550eb3836bf4eb782a5eae4bf274b
https://doi.org/10.4028/www.scientific.net/amr.634-638.970
https://doi.org/10.4028/www.scientific.net/amr.634-638.970
Publikováno v:
Advanced Materials Research. :3037-3040
A series of 13-cis-retinoate aryl derivatives were synthesized from 13-cis-retinoic acid and phenols or arylalcohol with dicyclohexylcarbodiimide (DCC) as reagent and 4-dimethylaminopyridine (DMAP) as catalyst. Their structures were characterized by1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30d7885e1655a29bb4370adbc516a47c
https://doi.org/10.4028/www.scientific.net/amr.236-238.3037
https://doi.org/10.4028/www.scientific.net/amr.236-238.3037
Publikováno v:
Advanced Materials Research. :2794-2797
In order to improve the therapeutic efficacy of retinoid carboxylic acids, a novel retinoate was designed and synthesized with 4-aminophenol as a linker from solanesol and 13-cis-retinoic acid. The synthetic procedure and characterization of the reti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc58adae22bc7949c3a6317a65d817b7
https://doi.org/10.4028/www.scientific.net/amr.236-238.2794
https://doi.org/10.4028/www.scientific.net/amr.236-238.2794
Publikováno v:
Advanced Materials Research. :1779-1782
Two series of novel organotin retinoates were synthesized by the reaction of di-n-butyltin oxide with corresponding retinoids in 1: 2 (3a~3d) and 1: 1 (4a~4d) molar ratio. These organotin retinoates were characterized by (1H,13C,119Sn) NMR, MS and IR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::046d61ed40523d1eab3ad40c0e2f225d
https://doi.org/10.4028/www.scientific.net/amr.236-238.1779
https://doi.org/10.4028/www.scientific.net/amr.236-238.1779