Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Cang Cheng"'
Publikováno v:
Organic Chemistry Frontiers. 9:4937-4942
A Pd-catalyzed cross-coupling reaction of 2-iodobiphenyls with ortho-chloroacetophenones has been developed through C–H activation. The reaction provides a straightforward method for the construction of tribenzo[a,c,f]cyclooctanones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aea20917c5480a7e4be14e92a84ad15f
https://doi.org/10.1039/d2qo00647b
https://doi.org/10.1039/d2qo00647b
Autor:
Cang Cheng, Yanghui Zhang
Publikováno v:
Organic Letters. 23:5772-5776
A Pd-catalyzed trans-selective carbosilylation reaction of alkynes has been developed. The trans-vinylpalladium species, generated through intramolecular syn-carbopalladation of alkynes and subsequent cis-trans isomerization, were captured by hexamet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f7da8dfd65c2640e390417f9bf47af4
https://doi.org/10.1021/acs.orglett.1c01931
https://doi.org/10.1021/acs.orglett.1c01931
Publikováno v:
Organic Letters. 23:1269-1274
A palladium-catalyzed cross-coupling reaction of 2-alkylphenyl bromides with biphenylene has been developed. The reactions formed eight-membered carbocycles through C(sp3)-H activation and the formation of two C-C bonds, and the chiral products were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f03d3b369023270a3cfc8770dac909b0
https://doi.org/10.1021/acs.orglett.0c04244
https://doi.org/10.1021/acs.orglett.0c04244
Publikováno v:
Organic Letters. 23:1239-1242
A novel and straightforward approach for the synthesis of tribenzo[b,d,f]azepines starting from 2-iodobiphenyls and 2-bromoanilines has been developed. A wide range of tribenzo[b,d,f]azepines were obtained in good to excellent yields via a cascade in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af6c091f7db6a31e77389fdd18de7c91
https://doi.org/10.1021/acs.orglett.0c04192
https://doi.org/10.1021/acs.orglett.0c04192
Publikováno v:
Chemical Communications. 57:2939-2942
A method for the synthesis of enantiopure eight-membered nitrogen heterocycles has been developed through diastereoselective cross-coupling of 2-iodobiphenyls with 2-bromobenzylamines. The products represent a novel type of chiral scaffold, which fea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5843428fa60898b323a664e697841a9
https://doi.org/10.1039/d1cc00398d
https://doi.org/10.1039/d1cc00398d
Publikováno v:
Advanced Synthesis & Catalysis. 362:1496-1501
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::981a51bce444546953d50bf6059cd813
https://doi.org/10.1002/adsc.201901372
https://doi.org/10.1002/adsc.201901372
Publikováno v:
Chemical communications (Cambridge, England). 57(76)
A palladium-catalyzed remote C-H silylation reaction has been developed through vinylic to aryl 1,4-palladium migration. By using alkyne-tethered aryl iodides as the starting materials and hexamethyldisilane as the silylating reagent, the reaction in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f80d78c0034eefed2005ea19328b4a8e
https://pubmed.ncbi.nlm.nih.gov/34555133
https://pubmed.ncbi.nlm.nih.gov/34555133
Publikováno v:
Chemical Communications. 56:7801-7804
A Pd(ii)-catalyzed intermolecular C-H silylation reaction initiated by aminopalladation has been developed. The C-H bonds were activated by an alkyl Pd(ii) species generated through aminopalladation and then disilylated with hexamethyldisilane to for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d6d438f6070657cee09deb9a63c1c4d
https://doi.org/10.1039/d0cc00872a
https://doi.org/10.1039/d0cc00872a
Synthesis of Indolines by Palladium-Catalyzed Intermolecular Amination of Unactivated C(sp3)–H Bonds
Publikováno v:
Organic Letters. 21:6508-6512
A new palladium-catalyzed C(sp3)-H amination reaction has been developed. 1-(tert-Butyl)-2-iodobenzene and its derivatives undergo palladium-catalyzed C-H activation to form palladacycles. The palladacycles are aminated with diaziridinone to form ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e984a4f548172eb13131f0e400d582d
https://doi.org/10.1021/acs.orglett.9b02386
https://doi.org/10.1021/acs.orglett.9b02386
Autor:
Cang, Cheng, Yanghui, Zhang
Publikováno v:
Organic letters. 23(15)
A Pd-catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ad69851987aa64f4e5e0a1f94916dd2
https://pubmed.ncbi.nlm.nih.gov/34259535
https://pubmed.ncbi.nlm.nih.gov/34259535