Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sheng‐Qi Qiu"'
Autor:
Sheng‐Qi Qiu, Yu Chen, Xiang‐Jun Peng, Shi‐Jiang He, Jun Kee Cheng, Yong‐Bin Wang, Shao‐Hua Xiang, Jun Song, Peiyuan Yu, Junmin Zhang, Bin Tan
Publikováno v:
Angewandte Chemie International Edition. 61
The application of Suzuki-Miyaura coupling reaction to forge the atropisomeric biaryls has seen remarkable progress but exploration of this chemistry to directly forge chiral C(aryl)-C(alkene) axis is underdeveloped. The replacement of arene substrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf1a240db57bca40025dfea05a50a4c3
https://doi.org/10.1002/anie.202211211
https://doi.org/10.1002/anie.202211211
Publikováno v:
Angewandte Chemie (International ed. in English). 62(1)
Anthrones and analogues are structural cores shared by diverse pharmacologically active natural and synthetic compounds. The sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e38bb9dc05c6b3c57db95f27a960db
https://pubmed.ncbi.nlm.nih.gov/36346195
https://pubmed.ncbi.nlm.nih.gov/36346195
Autor:
Wen Bao, Junmin Zhang, Shaoyu Li, Shao-Hua Xiang, Junxian Yang, Jun Song, Bin Tan, Ji-Wei Zhang, Sheng-Qi Qiu
Publikováno v:
Journal of the American Chemical Society. 143(33)
The previously elusive catalytic enantioselective construction of axially chiral B-aryl-1,2-azaborines with a C-B stereogenic axis has been realized through a chiral phosphoric acid-catalyzed desymmetrization strategy reported herein. The electrophil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a980eb411c1b97ce16b21212a1ac3554
https://pubmed.ncbi.nlm.nih.gov/34384026
https://pubmed.ncbi.nlm.nih.gov/34384026
Publikováno v:
Organic & Biomolecular Chemistry. 17:6122-6126
A copper-catalyzed regioselective 1,4- and 1,6-conjugate addition of a silyl reagent to diendioates was established. Various 1,4- and 1,6-protosilylation products were obtained in good yields and with high regioselectivity via tuning the ligands used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::361877e50082566076e772bb0034f73e
https://doi.org/10.1039/c9ob01086f
https://doi.org/10.1039/c9ob01086f
Publikováno v:
The Journal of organic chemistry. 84(11)
A Pd(II)-catalyzed mild and highly regioselective 6- endo cyclization/allylation reaction of enynoates with simple allylic alcohols has been developed. Under mild reaction conditions, the vinyl palladium species generated in situ after cyclization co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a89a9051c30ea279f8ef48a7bb17d4d
https://pubmed.ncbi.nlm.nih.gov/31081618
https://pubmed.ncbi.nlm.nih.gov/31081618
Palladium-Catalyzed Intermolecular Oxyarylation of Vinylacetates with Retention of an Alkenyl Moiety
Publikováno v:
Organic Letters. 17:3462-3465
Palladium-catalyzed intermolecular oxyarylation reaction of vinylacetates with retention of the double bond in the final product is developed. Under the optimized reaction conditions, the desired products of multisubstituted vinylesters could be obta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::642d3173c25b98e135751ca3d33f777e
https://doi.org/10.1021/acs.orglett.5b01507
https://doi.org/10.1021/acs.orglett.5b01507
Publikováno v:
ChemInform. 46
Palladium-catalyzed intermolecular oxyarylation reaction of vinylacetates with retention of the double bond in the final product is developed. Under the optimized reaction conditions, the desired products of multisubstituted vinylesters could be obta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d34092d82743192f95110248d400578e
https://doi.org/10.1002/chin.201552085
https://doi.org/10.1002/chin.201552085