Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ziqing Zuo"'
"2000年8月"
論文 (哲學碩士)--香港中文大學, 2000.
參考文獻 (leaves 155-162)
"2000 nian 8 yue"
Guo Shiyong.
Lun wen (zhe xue shuo shi)--Xianggang Zhong wen da xue, 2000.
Can kao wen xian (leaves 155-162)<
論文 (哲學碩士)--香港中文大學, 2000.
參考文獻 (leaves 155-162)
"2000 nian 8 yue"
Guo Shiyong.
Lun wen (zhe xue shuo shi)--Xianggang Zhong wen da xue, 2000.
Can kao wen xian (leaves 155-162)<
Externí odkaz:
http://library.cuhk.edu.hk/record=b5890516
http://repository.lib.cuhk.edu.hk/en/item/cuhk-323293
http://repository.lib.cuhk.edu.hk/en/item/cuhk-323293
Publikováno v:
ACS Omega, Vol 2, Iss 8, Pp 4688-4692 (2017)
Externí odkaz:
https://doaj.org/article/15ce38c90ac3421db893a3cab1cb9920
Publikováno v:
Organometallics. 38:3906-3911
The asymmetric hydrogenation of vinylsilanes catalyzed by a new C1-symmetric phosphine–pyridine–oxazoline cobalt complex is described. The method provides an efficient approach to chiral tertiary s...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f9e54b7a50f80bcc6c640dca423d247
https://doi.org/10.1021/acs.organomet.9b00067
https://doi.org/10.1021/acs.organomet.9b00067
Publikováno v:
J Am Chem Soc
We report an asymmetric Ullmann-type homocoupling of ortho-(iodo)arylphosphine oxides and ortho-(iodo)arylphosphonates that results in highly enantioenriched axially chiral bisphosphine oxides and bisphosphonates in good yields and excellent enantios
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a47dc57075dc9b9ba7ec7d275e6263df
https://pubmed.ncbi.nlm.nih.gov/33439640
https://pubmed.ncbi.nlm.nih.gov/33439640
We report an asymmetric Ullmann-type homocoupling of ortho-(iodo)arylphosphine oxides and ortho-(iodo)arylphosphonates that results in highly enantioenriched axially chiral bisphosphine oxides and bisphosphonates in good yields and excellent enantios
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7cf4a1ddb9bd16fb38b692eeb87ed44
https://doi.org/10.26434/chemrxiv.13003073
https://doi.org/10.26434/chemrxiv.13003073
Publikováno v:
Synlett. 29:1421-1429
Incorporation of the boryl moiety across a carbon–carbon multiple bond is a powerful method for the synthesis of organoboron compounds. This kind of transformation could be realized with high chemo-, regio-, and stereoselectivity by using an approp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bda2e82c62d5c4ff00b734f7ee37cc2
https://doi.org/10.1055/s-0037-1609682
https://doi.org/10.1055/s-0037-1609682
Publikováno v:
ACS Omega
ACS Omega, Vol 2, Iss 8, Pp 4688-4692 (2017)
ACS Omega, Vol 2, Iss 8, Pp 4688-4692 (2017)
We disclose the synthesis of a series of manganese complexes of chiral iminopyridine oxazoline ligands and their application in the first manganese-catalyzed asymmetric ketone hydrosilylations. The most sterically hindered manganese catalyst bearing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ffb9a7b25c9a9aa1f0a2306bde0c9a
http://europepmc.org/articles/PMC6641774
http://europepmc.org/articles/PMC6641774
Autor:
Zheng Huang, Ziqing Zuo
Publikováno v:
Organic Chemistry Frontiers. 3:434-438
A cobalt complex of iminopyridine-oxazoline catalyzes sequential hydroboration of alkyl and aryl alkynes with pinacolborane to form 1,1-diboronate esters. The reactions proceed under mild conditions with high yields, high regioselectivity, and wide f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43d3204258a0c18fc491aacfd8772ad3
https://doi.org/10.1039/c5qo00426h
https://doi.org/10.1039/c5qo00426h
Publikováno v:
Journal of the American Chemical Society. 136:15501-15504
We report the synthesis of cobalt complexes of novel iminopyridine-oxazoline (IPO) ligands and their application to the asymmetric hydroboration of 1,1-disubstituted aryl alkenes. The new catalysts afforded α-alkyl-β-pinacolatoboranes with exclusiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::343ac949a5d7b20f7c42f3e8471c6692
https://doi.org/10.1021/ja5093908
https://doi.org/10.1021/ja5093908
Publikováno v:
Angewandte Chemie. 126:2734-2738
An extremely efficient cobalt catalyst for the hydroboration of both vinylarenes and aliphatic α-olefins with pinacolborane is described, providing the anti-Markovnikov products with excellent regio- and chemoselectivity, broad functional-group tole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28119624e1c3b0f38cfcd0d5425adcdc
https://doi.org/10.1002/ange.201310096
https://doi.org/10.1002/ange.201310096