Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Jianrong Steve, Zhou"'
Publikováno v:
Journal of the American Chemical Society; 7/24/2024, Vol. 146 Issue 29, p20477-20493, 17p
Autor:
Luoqiang Zhang, Dao-Yong Zhu, Jingyao Hu, Minjun Feng, Tze Chien Sum, Haoran Sun, Hajime Hirao, Yonggui Robin Chi, Jianrong Steve Zhou
Publikováno v:
Organic Chemistry Frontiers. 10:1651-1659
Azole and azine heteroarenes were directly alkylated by alkanes, ethers, or carbamates using PhC(O)O2tBu under LED irradiation. 9,10-Dichloroanthrocene acted as an organic photocatalyst and transferred its excitation energy to PhC(O)O2tBu via exciple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4848ceaaa34a6a28326ebabc876e3b6
https://doi.org/10.1039/d2qo01558g
https://doi.org/10.1039/d2qo01558g
Publikováno v:
Chemical Science. 14:3010-3017
Catalytic domino alkenylation–heteroarylation of nonconjugated iododienes proceeded with excellent stereoselectivity and broad scope of substrates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eb21bffb6b0b94c09ce5fe154369582
https://doi.org/10.1039/d2sc07117g
https://doi.org/10.1039/d2sc07117g
Publikováno v:
Organic Letters. 24:6520-6524
Pd-catalyzed chemo- and regiocontrollable 1,1-diarylation of unactivated aliphatic alkenes with two aryl halides was developed. Under the cationic reductive-delay Heck pathway, the first aryl insertion is followed by β-H elimination, while the secon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d917bcda26bacd53cf175b0df19fbd5
https://doi.org/10.1021/acs.orglett.2c02416
https://doi.org/10.1021/acs.orglett.2c02416
Autor:
Aibo Li, Xinjian Song, Qiao Ren, Peiwang Bao, Xinyu Long, Fuli Huang, Lvjiang Yuan, Jianrong Steve Zhou, Xurong Qin
Publikováno v:
Angewandte Chemie International Edition. 62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::221a54de42bcd3beb94de0d8189ad4d2
https://doi.org/10.1002/anie.202301091
https://doi.org/10.1002/anie.202301091
Publikováno v:
Science China Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65391cd1b58ad84812cb9c18243092b1
https://doi.org/10.1007/s11426-023-1552-0
https://doi.org/10.1007/s11426-023-1552-0
Autor:
Luoqiang Zhang, Xiuhua Wang, Maoping Pu, Caiyou Chen, Peng Yang, Yun-Dong Wu, Yonggui Robin Chi, Jianrong Steve Zhou
Publikováno v:
Journal of the American Chemical Society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b43750bd1e4d98d6409b87c321f9e83e
https://doi.org/10.1021/jacs.3c00548
https://doi.org/10.1021/jacs.3c00548
Autor:
Jianrong Steve Zhou, Shenghan Teng
Publikováno v:
Chemical Society Reviews. 51:1592-1607
This review summarizes the state-of-the-art in transition metal-catalyzed asymmetric alkylation of heteroarenes using alkenes (covering literature from 2000 to late 2021). Based on elementary reactions on metals for substrate activation, these reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbbb8670954225272525e6c3c2cbd023
https://doi.org/10.1039/d1cs00426c
https://doi.org/10.1039/d1cs00426c
Publikováno v:
Organic letters. 24(24)
A nickel-catalyzed intermolecular arylcyanation of 8-aminoquinolinyl β,γ-unsaturated amides is reported. The three-component reaction directly afforded diverse β-cyano γ-aryl amides with exclusive chemo- and regioselectivity. The synthetic practi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::199c501d34b43463ed9b373cf9f15718
https://pubmed.ncbi.nlm.nih.gov/35686833
https://pubmed.ncbi.nlm.nih.gov/35686833
Autor:
Yonggui Robin Chi, Maoping Pu, Shenghan Teng, Yun-Dong Wu, Wenqiang Xu, Xiaolei Huang, Jianrong Steve Zhou
Publikováno v:
Angewandte Chemie. 133:2864-2868
Nickel-catalyzed intermolecular Heck reaction of cycloalkenes proceeds well with aryl triflates, mesylates and tosylates in excellent enantiomeric ratios. The asymmetric reductive Heck reaction also works with a 2-cyclopentenone ketal, which is equiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a58e8349b644bd5b61a13d5c84b206e4
https://doi.org/10.1002/ange.202011036
https://doi.org/10.1002/ange.202011036