Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Qiwen Hou"'
Publikováno v:
2016 35th Chinese Control Conference (CCC).
In this paper, we propose an improved part-based tracking method based on compressive tracker. The traditional compressive tracking can hardly deal with occlusion and scale variation, which is not robust enough in these situations. In our part-based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18b1c755241faa3bf4a1f22da40ee16c
https://doi.org/10.1109/chicc.2016.7553974
https://doi.org/10.1109/chicc.2016.7553974
Publikováno v:
Synthesis. 2011:626-634
An expedient approach was developed to construct the 11 H-indolo[3,2- C]quinolinescaffold starting from acyclic alkyne substrates. The five- andsix-membered nitrogen-containing rings in the tetracyclic skeletonwere elaborated efficiently by gold(III)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8155e0e06cc09dbf6df55eb7e416b4f
https://doi.org/10.1055/s-0030-1258411
https://doi.org/10.1055/s-0030-1258411
Publikováno v:
ChemInform. 44
A tandem reaction initiated by Au(I)-catalyzed C1—C5 cyclization of enediynes (I) and (III) bearing an internal carboxy nucleophile is developed, providing a novel route for the assembly of fused indene derivatives (II) and (IV).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dc2785a587d00466f27ed1f1698655f
https://doi.org/10.1002/chin.201320155
https://doi.org/10.1002/chin.201320155
Publikováno v:
Chemical communications (Cambridge, England). 49(7)
A tandem reaction initiated by Au(I)-catalyzed C1–C5 cyclization of enediynes bearing an internal carboxy nucleophile has been developed, providing a distinctive methodology for the assembly of fused indenes including indeno[1,2-c]isochromen-5(11H)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a94bba1136283c6517c54636d1f3002
https://pubmed.ncbi.nlm.nih.gov/23223174
https://pubmed.ncbi.nlm.nih.gov/23223174
Publikováno v:
ChemInform. 42
The sequence involves 2 cyclization steps, where the second one is promoted by the Hendrickson reagent (Ph3P-O-PPh3)(Tf-O)2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4f107f2ce2f989ecbc333d82445bf79
https://doi.org/10.1002/chin.201120148
https://doi.org/10.1002/chin.201120148
Publikováno v:
ChemInform. 42
The metal-free protocol features mild conditions for installation of an iodine atom on the azaanthraquinone ring and benign functional group compatibility.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5367aa794da4c9d3931fc1b70a8bdef0
https://doi.org/10.1002/chin.201105150
https://doi.org/10.1002/chin.201105150
Publikováno v:
Organicbiomolecular chemistry. 8(18)
An efficient methodology taking advantage of the excellent nucleophilicity of aminoquinone to assemble the azaanthraquinone framework was developed via an iodine-induced 6-endo-dig electrophilic cyclization. Therefore, starting from N-propargylaminoq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a5060a27ddc9b07edc343c9037ab2cc
https://pubmed.ncbi.nlm.nih.gov/20652179
https://pubmed.ncbi.nlm.nih.gov/20652179
Publikováno v:
Synthesis; 2011, Vol. 2011 Issue 4, p626-634, 9p
Publikováno v:
Organic & Biomolecular Chemistry; 9/21/2010, Issue 18, p4096-4103, 8p