Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Xiang Yi Bin"'
Autor:
Xiang Yi-bin
Publikováno v:
Cluster Computing. 22:6599-6607
The development of quantum technology has a profound influence on the research of consciousness. Through the analysis of the interaction of various microscopic particles in the universe, the article put forward that all things have an interconnected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b1f27bf60af7bf2053c1560d4ee2b36
https://doi.org/10.1007/s10586-018-2354-1
https://doi.org/10.1007/s10586-018-2354-1
Autor:
Xiang Yi-bin
Publikováno v:
Wireless Personal Communications. 95:2021-2032
Quantum communication is the current hot topic of complex networks. This article discusses interactions between various fields in quantum field theory, relationship between Compton wavelength and Schwarzschild radius, and the impact of quantum entang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::507601348ca8f62c328767041b780467
https://doi.org/10.1007/s11277-016-3926-0
https://doi.org/10.1007/s11277-016-3926-0
Autor:
Marc Labelle, Paul J. Reider, Jacques Yves Gauthier, Paul Davis, Robert D. Larsen, Edward G. Corley, James D. Carroll, Xiang Yi Bin, Robert Zamboni, Anthony O. King, Thomas R. Verhoeven
Publikováno v:
The Journal of Organic Chemistry. 61:3398-3405
A general approach to the synthesis of a new class of LTD4 antagonists is presented. The key diarylpropane framework was prepared by Claisen−Schmidt condensation and selective reduction of the enone. Depending on the bridge to the 7-chloroquinaldin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcff54963243353d0266595b8e23503b
https://doi.org/10.1021/jo952103j
https://doi.org/10.1021/jo952103j
Autor:
M. Belley, Yves Leblanc, Kathleen M. Metters, M. McAuliffe, Nicole Sawyer, Claude Dufresne, Anthony W. Ford-Hutchinson, Robert Zamboni, Deborah Slipetz, Thomas R. Jones, Cheuk K. Lau, Robert N. Young, C.B. Pickett, C. Rochette, C. S. Mcfarlane, Zhaoyin Wang, Helene Perrier, Nathalie Ouimet, Marc Labelle, Yves Gareau, Xiang Yi Bin
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:2551-2556
Structure-activity studies leading to the discovery of a new series of non-quinoline cysLT 1 receptor (LTD 4 receptor) antagonists are described. These studies demonstrated that the quinoline ring system of montelukast ( 5 ) may be replaced by an app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::205a495753e4e61eaaa19bad61cf9e8e
https://doi.org/10.1016/0960-894x(95)00448-3
https://doi.org/10.1016/0960-894x(95)00448-3
Autor:
Robert D. Larsen, Xiang Yi Bin, Anthony O. King, R. K. Anderson, Thomas R. Verhoeven, M. Belley, Paul J. Reider, Edward G. Corley, Yves Leblanc
Publikováno v:
The Journal of Organic Chemistry. 58:3731-3735
The asymmetric synthesis of L-699,392 (1) [3-[[(1S)-[3(E)-[2-(7-chloroquinolinyl)ethenyl]phenyl]- 3-(acetylphenyl)propyl]thio]-2(S)-methylpropanoic acid], a leukotriene antagonist, is accomplished in six steps starting from the monoaldehyde 2, 3-[2-(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bceee0f7834c2c94fa85fa196ca3b8b8
https://doi.org/10.1021/jo00066a027
https://doi.org/10.1021/jo00066a027
Publikováno v:
ChemInform. 23
The chiral ester 1 was enolized under TiCl 4 /Et 3 N conditions and reacted with aldehydes to give moderate to good stereoselectivities. The chiral auxiliary group can be removed by simple saponification and recovered.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::942d14a26f33044a4045315ccd9a4278
https://doi.org/10.1002/chin.199235064
https://doi.org/10.1002/chin.199235064
Autor:
Yves Leblanc, Robert N. Young, Helene Perrier, Claude Dufresne, Cheuk K. Lau, C. S. Mcfarlane, Thomas R. Jones, Kathleen M. Metters, Robert Zamboni, C.B. Pickett, Marc Labelle, Anthony W. Ford-Hutchinson, Nicole Sawyer, Nathalie Ouimet, Deborah Slipetz, M. McAuliffe, Zhaoyin Wang, C. Rochette, Yves Gareau, Xiang Yi Bin, M. Belley
Publikováno v:
ChemInform. 27
Structure-activity studies leading to the discovery of a new series of non-quinoline cysLT 1 receptor (LTD 4 receptor) antagonists are described. These studies demonstrated that the quinoline ring system of montelukast ( 5 ) may be replaced by an app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f48c6bedddbe5c1115c4629f8deaccb
https://doi.org/10.1002/chin.199609156
https://doi.org/10.1002/chin.199609156
Autor:
Thomas R. Verhoeven, Anthony O. King, Paul J. Reider, Paul Davis, Edward G. Corley, James D. Carroll, Xiang Yi Bin, Marc Labelle, Robert Zamboni, Jacques Yves Gauthier, Robert D. Larsen
Publikováno v:
ChemInform. 27
A general approach to the synthesis of a new class of LTD4 antagonists is presented. The key diarylpropane framework was prepared by Claisen−Schmidt condensation and selective reduction of the enone. Depending on the bridge to the 7-chloroquinaldin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce0cdf46ac53dac10241aed8461e9b82
https://doi.org/10.1002/chin.199637198
https://doi.org/10.1002/chin.199637198
Publikováno v:
Tetrahedron Letters. 33:457-460
The chiral ester 1 was enolized under TiCl 4 /Et 3 N conditions and reacted with aldehydes to give moderate to good stereoselectivities. The chiral auxiliary group can be removed by simple saponification and recovered.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e58ce606d1279b4f745ba6f224454207
https://doi.org/10.1016/s0040-4039(00)93967-4
https://doi.org/10.1016/s0040-4039(00)93967-4
Publikováno v:
The Journal of Organic Chemistry. 58:993-994
A method for preparation of enantiomerically pure α-hydroxy esters by stereoselective reduction of chiral α-keto ester under convenient conditions (LiAlH(OCEt 3 ) 3 , THF, 0 o C) has been developed. The compounds exo,exo-3-(arysulfonamido)-2-borneo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3301c39b7484635346cb8bc401786870
https://doi.org/10.1021/jo00057a004
https://doi.org/10.1021/jo00057a004