Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Yan Ying Zhu"'
Autor:
Dun Wang, Sheng Yang, Kai-Xuan Guo, Yan-Ying Zhu, Jia Sun, Aliona Dreglea, Yan-Hong Gao, Jiao Yu
Publikováno v:
Medicine in Novel Technology and Devices, Vol 19, Iss , Pp 100248- (2023)
It is difficult to use a single edge operator in image processing to extract continuous and accurate contours of a porous bioelastomer due to the fuzzy boundary and complex background in ultrasound images. To solve this problem, this paper proposes a
Externí odkaz:
https://doaj.org/article/a7033a690937498d8bef76da72e62bb2
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract In this paper, the surface enhanced Raman scattering (SERS) characteristics of Au and Au@Al2O3 nanoparticle dimers were calculated and analyzed by using finite element method (3D-FEM). Firstly, the electric field enhancement factors of Au na
Externí odkaz:
https://doaj.org/article/85ea3097f6124aa4bf7b6cacfc9a74c2
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Abstract A flexible and stable biomimetic SERS substrate was successfully fabricated by depositing gold (Au) nanoislands on the dragonfly wings (DW) via a simple DC magnetron sputtering system. Characterizations of the Au/DW nanostructure indicated t
Externí odkaz:
https://doaj.org/article/dd579ebab7f642029bb9e5f02b5fc285
Publikováno v:
Quantum Information Processing. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a970f73f1cddc418946973a76c89bbb9
https://doi.org/10.1007/s11128-022-03601-x
https://doi.org/10.1007/s11128-022-03601-x
Publikováno v:
Asian Journal of Organic Chemistry. 10:1410-1413
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36a5defa90eec21ca6712b6b01b00934
https://doi.org/10.1002/ajoc.202100159
https://doi.org/10.1002/ajoc.202100159
Publikováno v:
Physica A: Statistical Mechanics and its Applications. 619:128734
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2744b13938295d16febab3823e339cf8
https://doi.org/10.1016/j.physa.2023.128734
https://doi.org/10.1016/j.physa.2023.128734
Publikováno v:
Organic Letters. 22:2060-2063
The first example of Ir(III)-catalyzed C–H activation/cyclization with N-alkoxyamides as amidation reagents to simultaneously form functionalized thiadiazine 1-oxide derivatives was developed. This...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4263366fea2a8ecf5ae2d074dd71c3e3
https://doi.org/10.1021/acs.orglett.0c00520
https://doi.org/10.1021/acs.orglett.0c00520
RhIII-Catalyzed one-pot cascade synthesis of quinazolines with N-alkoxyamide as an amidating reagent
Publikováno v:
Organic Chemistry Frontiers. 7:1230-1234
Novel and efficient rhodium(III)-catalyzed C–H bond activation and tandem annulation for the synthesis of structurally complex quinazolines have been successfully developed. N-alkoxyamide as an amidating reagent was first used to construct this het
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a48343122e7726ae6417946577d18db
https://doi.org/10.1039/d0qo00084a
https://doi.org/10.1039/d0qo00084a
Publikováno v:
The Journal of Organic Chemistry. 84:16286-16292
An efficient synthetic method to construct 3H-indole derivatives has been successfully developed involving rhodium-catalyzed highly selective C-H bond activation of N-phenylbenzimidamides and subsequent couplings with pyridotriazoles. This cascade ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f55516a3b6c72072950923e3c940d6e
https://doi.org/10.1021/acs.joc.9b02468
https://doi.org/10.1021/acs.joc.9b02468
Publikováno v:
Organic Chemistry Frontiers. 6:3864-3867
Rhodium(III)-catalyzed double C–H activation and in situ dealcoholization to generate useful biheteroaryl-2-carbonitriles have been well developed via a CDC mechanism, in which benzimidates act as both directing groups and the precursors of nitrile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec7a7e14ed8ed2e1687e3ca5fcf45c8e
https://doi.org/10.1039/c9qo01114e
https://doi.org/10.1039/c9qo01114e