Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Ming-Zhong Cai"'
Publikováno v:
ARKIVOC, Vol 2008, Iss 16, Pp 92-98 (2008)
Externí odkaz:
https://doaj.org/article/82a5975ae37140e7a266c66c5afef551
Publikováno v:
ARKIVOC, Vol 2008, Iss 2, Pp 287-293 (2008)
Externí odkaz:
https://doaj.org/article/8b7ee4efb8d7475da5a235bc84fbe25e
Publikováno v:
Chemical Engineering Journal. 435:134876
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84d8977254b91cf2cdb83aa44671cd35
https://doi.org/10.1016/j.cej.2022.134876
https://doi.org/10.1016/j.cej.2022.134876
Publikováno v:
Chinese Chemical Letters. 21:1310-1313
The hydrosilylation of alkenes with triethoxysilane has been achieved at 120 °C in the presence of 0.01 mol% of thioether-functionalized MCM-41 anchored rhodium complex, affording the corresponding addition products in 68–91% yields. This supporte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54c62551d90d648faa1408bb7d3605d4
https://doi.org/10.1016/j.cclet.2010.06.007
https://doi.org/10.1016/j.cclet.2010.06.007
Publikováno v:
Chinese Chemical Letters. 19:1047-1050
1,4-Dienyl selenides can be stereoselectively synthesized in one pot under mild conditions in good yields by the palladium-catalyzed hydrostannylation of acetylenic selenides, followed by Stille coupling with allylic bromides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e2ab2b3a6788824faf9486a29502f81
https://doi.org/10.1016/j.cclet.2008.06.029
https://doi.org/10.1016/j.cclet.2008.06.029
Publikováno v:
Chinese Chemical Letters. 19:783-787
A variety of terminal arylacetylenes have been conveniently synthesized in good to high yields via Sonogashira coupling of aryl iodides with (trimethylsilyl)acetylene catalyzed by MCM-41-supported mercapto palladium(0) complex, followed by desilylati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c99f8421480424bb323b34572bca6dec
https://doi.org/10.1016/j.cclet.2008.05.016
https://doi.org/10.1016/j.cclet.2008.05.016
Publikováno v:
ARKIVOC, Vol 2008, Iss 2, Pp 287-293 (2008)
Acylation of polystyrene-supported α-selenopropionic acid with acid hydrazides, followed by cyclocondensation with arylphosphazoanilides, and oxidation-elimination with 30 % hydrogen peroxide efficiently afforded vinyl-substituted 1,2,4-triazoles in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73753602c730e0131d04577b11f61f86
https://doi.org/10.3998/ark.5550190.0009.230
https://doi.org/10.3998/ark.5550190.0009.230
Publikováno v:
Chinese Journal of Chemistry. 25:1927-1931
(E)-α-Stannylvinyl phenyl(or p-tolyl)sulfones underwent an iododestannylation reaction to afford (E)-α-iodovinyl phenyl(or p-tolyl)sulfones 1, which reacted with (E)-alkenylzirconium(IV) complexes 2 produced in situ by hydrozirconation of terminal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b2d9d97e27625d5a2ffdbc49194a27c
https://doi.org/10.1002/cjoc.200790355
https://doi.org/10.1002/cjoc.200790355
Publikováno v:
Chinese Chemical Letters. 18:773-776
( E )-α-Iodovinyl sulfones 1 underwent the Sonogashira coupling reactions with terminal alkynes 2 in piperidine at room temperature in the presence of 5 mol% of Pd(PPh 3 ) 4 and 10 mol% of CuI to stereospecifically afford the corresponding ( Z )-2-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94de2690775281d158672defaa9db7c1
https://doi.org/10.1016/j.cclet.2007.05.021
https://doi.org/10.1016/j.cclet.2007.05.021
Publikováno v:
Chinese Chemical Letters. 18:387-389
Various functionalized asymmetrical biaryls can be synthesized in high to excellent yields via coupling reaction of aryl iodides or bromides with NaBPh4 catalyzed by MCM-41-supported sulfur palladium(0) complex. This palladium complex can be easily r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b09a2707bb46bf23b1efe2c6d21ada6d
https://doi.org/10.1016/j.cclet.2007.01.046
https://doi.org/10.1016/j.cclet.2007.01.046