Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Gui-Jun Sun"'
Publikováno v:
Advanced Synthesis & Catalysis. 360:1790-1794
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63e2db49f3d4e6d690a4892723cc88f5
https://doi.org/10.1002/adsc.201800021
https://doi.org/10.1002/adsc.201800021
Publikováno v:
Advanced Synthesis & Catalysis. 360:1094-1098
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c7e6da19912bcfce30703e804fab621
https://doi.org/10.1002/adsc.201701377
https://doi.org/10.1002/adsc.201701377
Publikováno v:
Chinese Journal of Chemistry. 36:20-24
A highly regio-, diastereo- and enantioselective addition of 2-acyl imidazoles or 2-acyl pyridines with allenes promoted by Rh/Lewis acid synergistically catalytic system is described. This atom economic approach leads to the formation of the branche
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d90ff849d79f89adc4c8367a312c9af9
https://doi.org/10.1002/cjoc.201700596
https://doi.org/10.1002/cjoc.201700596
Publikováno v:
The Journal of Organic Chemistry. 82:796-803
Chiral Rh(III) complex catalyzed highly efficient enantioselective cyclopropanation of α,β-unsaturated 2-acyl imidazoles or pyridine with 2-bromomalonate is developed to generate corresponding multisubstituted cyclopropanes in 70-99% yields with 93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5240a091a64ee88e67bc527d246eb0c7
https://doi.org/10.1021/acs.joc.6b02583
https://doi.org/10.1021/acs.joc.6b02583
Autor:
Zixiao Huang, Yang Yang, Shengrong Wu, Xiangyi He, Jiajia Jin, Xiaoyan Lu, Gui-Jun Sun, Qing Liu
The aims of this study were to generate periodontal ligament (PDL) cells that have adenovirus- or lentivirus-mediated overexpression of human telomerase reverse transcriptase (hTERT) and to compare the osteogenic and proliferative abilities of the tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::404a59433b3dc6c0186812c4b0ac29f6
https://europepmc.org/articles/PMC6486670/
https://europepmc.org/articles/PMC6486670/
Publikováno v:
Synthesis. 47:2931-2936
An efficient approach for palladium(II) acetate catalyzed allylic amination of homoallylic alcohols with various amines via sequential retro-allylation and amination was developed, which afforded the corresponding allylic amines in up to 98% yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf2f3c82d5b5a435acf8d7475e8e4919
https://doi.org/10.1055/s-0034-1380418
https://doi.org/10.1055/s-0034-1380418
Publikováno v:
Chemical communications (Cambridge, England). 53(54)
We report an efficient enantioselective conjugate addition of photogenerated α-amino radicals to Michael acceptors catalyzed by a newly prepared chiral-at-metal rhodium complex. This protocol shows that a single Rh(III) complex can serve not only as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eec1e959c22642b20dc793a8df75dd0
https://pubmed.ncbi.nlm.nih.gov/28643839
https://pubmed.ncbi.nlm.nih.gov/28643839
Publikováno v:
ChemInform. 47
A highly regio- and stereoselective Rh-catalyzed intermolecular head-to-head [2 + 2] cycloaddition of allenamides was developed. The intermolecular cycloadducts, trans-dimethylenecyclobutane-1,2-diamine derivatives, were achieved in good yields with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96b8ebdc3962a58c12b1875cfdf99125
https://doi.org/10.1002/chin.201650056
https://doi.org/10.1002/chin.201650056
Publikováno v:
Organic letters. 18(15)
A highly regio- and stereoselective Rh-catalyzed intermolecular head-to-head [2 + 2] cycloaddition of allenamides was developed. The intermolecular cycloadducts, trans-dimethylenecyclobutane-1,2-diamine derivatives, were achieved in good yields with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70a768e296942ecc2fe4cfa347e91e7d
https://pubmed.ncbi.nlm.nih.gov/27403894
https://pubmed.ncbi.nlm.nih.gov/27403894
Publikováno v:
ChemInform. 47
An efficient approach for palladium(II) acetate catalyzed allylic amination of homoallylic alcohols with various amines via sequential retro-allylation and amination was developed, which afforded the corresponding allylic amines in up to 98% yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc9c367098deefe878d5902fe7602760
https://doi.org/10.1002/chin.201607095
https://doi.org/10.1002/chin.201607095