Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Zhanwei Bu"'
Publikováno v:
The Journal of Organic Chemistry. 86:13548-13558
An unexpected cleavage of the Csp3-CF3 bond of CF3-hydrobenzoxazoles has been disclosed, affording a range of 2-aryl benzoxazoles under metal-free and redox-neutral conditions. This transformation has demonstrated broad substrate scope and good compa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd32bb4f6b34a960cd5ab5232ab58a7a
https://doi.org/10.1021/acs.joc.1c01619
https://doi.org/10.1021/acs.joc.1c01619
Publikováno v:
Organic Chemistry Frontiers. 8:204-211
A highly diastereoselective multicomponent dearomative multifunctionalization of N-alkyl activated azaarenes with 1,5-diazapentadienium salts has been developed, which not only represented a significant advance in maximum utilization of the reactive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b40da36e103efb90fe58655173957b71
https://doi.org/10.1039/d0qo01196g
https://doi.org/10.1039/d0qo01196g
Publikováno v:
Chemical Communications. 57:359-362
Reported herein is an unexpected construction of functionalized π-extended indolizine polycycles through a one-pot two-step cascade process comprising the base-promoted dearomative [3+2] cycloaddition of quinilinium salts and 3-alkenyl oxindoles, fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fede6276a12cdf5605312b06fccbd5b5
https://doi.org/10.1039/d0cc07116a
https://doi.org/10.1039/d0cc07116a
Publikováno v:
Organic Letters. 22:5068-5073
Reported herein is an unprecedented multicomponent one-pot dearomative multifunctionalization of commercially available azaarenes through an in situ activation strategy, which not only achieved the first full exploitation of the reactive sites of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c010d8f633cbad0274556926a3d92f6
https://doi.org/10.1021/acs.orglett.0c01648
https://doi.org/10.1021/acs.orglett.0c01648
Publikováno v:
Organic Letters. 22:873-878
New chalcone-based pyridinium salts have been successfully exploited, which could smoothly participate in the highly diastereoselective dearomatization with binucleophilic enaminones by taking advantage of their multiple reactive sites to construct b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b519d57ff2f375f65d8a0fec2bff3a8a
https://doi.org/10.1021/acs.orglett.9b04398
https://doi.org/10.1021/acs.orglett.9b04398
Publikováno v:
Chemical Science. 11:1418-1424
An unprecedented base-promoted multi-component one-pot dearomatization of N-alkyl activated azaarenes was developed, which enabled the synthesis of complex and diverse bridged cyclic polycycles with multiple stereocenters in a highly regio- and diast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feba975cf09a0b1514a6cd7e468e36d3
https://doi.org/10.1039/c9sc04880d
https://doi.org/10.1039/c9sc04880d
Publikováno v:
Chemical communications (Cambridge, England). 57(74)
A highly diastereoselective dearomative trifunctionalization of pyridinium salts with multifunctional o-hydroxyl aromatic azomethine ylides has been established, which not only provided a convenient and rapid method to assemble challenging and archit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6504e975d2e063aeb6699a66223a9308
https://pubmed.ncbi.nlm.nih.gov/34528954
https://pubmed.ncbi.nlm.nih.gov/34528954
Publikováno v:
Chemical Communications. 55:5207-5210
An unexpected multi-component one-pot cascade reaction of hydroxyketones with ortho-hydroxychalcones has been developed to afford an array of new furanobenzopyran-fused polycyclic compounds with complex molecular architectures. This reaction not only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f1ad6b89f5356f199cd4ee2652ddb96
https://doi.org/10.1039/c9cc02170a
https://doi.org/10.1039/c9cc02170a
Publikováno v:
Organicbiomolecular chemistry. 19(18)
Bridged polycycles are privileged molecular skeletons with wide occurrence in bioactive natural products and pharmaceuticals. Therefore, they have been the pursing target molecules of numerous chemists. The rapid and convenient generation of sp3-rich
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3281242d3e2e6f96b5b25e0b3516da83
https://pubmed.ncbi.nlm.nih.gov/33978039
https://pubmed.ncbi.nlm.nih.gov/33978039
Publikováno v:
Advanced Synthesis & Catalysis. 361:456-461
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c237400846b4d2b3910ca85c5dc841a
https://doi.org/10.1002/adsc.201801227
https://doi.org/10.1002/adsc.201801227