Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Yuk Fai Wong"'
Publikováno v:
The Journal of Organic Chemistry. 88:2583-2588
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c36f7c03d2737b73c38ee7774c05e221
https://doi.org/10.1021/acs.joc.2c02614
https://doi.org/10.1021/acs.joc.2c02614
Publikováno v:
ISVLSI
Convolutional neural networks (CNNs) have achieved near or exceeding human performance in computer vision, yet their large computational and memory requirements made them difficult to deploy in both large data centers and embedded systems. CNNs are t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbb83810e7469f3c94781a0fa96893b0
https://doi.org/10.1109/isvlsi51109.2021.00048
https://doi.org/10.1109/isvlsi51109.2021.00048
Publikováno v:
Organic Letters. 21:7746-7749
A one-pot method for joining three separate components leading to an assortment of N-substituted 3,4-dihydro-2H-1,3-benzoxazines is described. The method involves the addition of a Grignard reagent to an o-OBoc salicylaldehyde in the presence of an i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a3521ef143c31db2d16d097a6e4fde4
https://doi.org/10.1021/acs.orglett.9b02655
https://doi.org/10.1021/acs.orglett.9b02655
Publikováno v:
Journal of the American Chemical Society. 139:16064-16067
An accelerative asymmetric gold catalysis is achieved for the first time via chiral ligand metal cooperation. An asymmetrically positioned remote amide group in the designed chiral binaphthyl-based ligand plays the essential role of a general base ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b6f7bdfd1ad7c15f3a4eec461fc9a51
https://doi.org/10.1021/jacs.7b09136
https://doi.org/10.1021/jacs.7b09136
Publikováno v:
Organic letters. 21(19)
A one-pot method for joining three separate components leading to an assortment of N-substituted 3,4-dihydro-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3930d7fefbd66383a4f245092f910e31
https://pubmed.ncbi.nlm.nih.gov/31532216
https://pubmed.ncbi.nlm.nih.gov/31532216
Publikováno v:
Tetrahedron. 72:2748-2751
A one-pot oxidation/cycloaddition cascade for the synthesis of 2,4-diaryl chromans is developed. The reaction involves in situ oxidative generation of the unstable o -quinone methides followed by endo selective [4+2] cycloaddition with styrenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e28e247ffd9c784b2dc4c30d5ef9142
https://doi.org/10.1016/j.tet.2015.12.011
https://doi.org/10.1016/j.tet.2015.12.011
Publikováno v:
ChemInform. 47
A one-pot oxidation/cycloaddition cascade for the synthesis of 2,4-diaryl chromans is developed. The reaction involves in situ oxidative generation of the unstable o -quinone methides followed by endo selective [4+2] cycloaddition with styrenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::200e01cfff85b8e70bda38ff823bd2b4
https://doi.org/10.1002/chin.201638153
https://doi.org/10.1002/chin.201638153
Publikováno v:
ChemInform. 47
Described herein is a general and mild catalytic asymmetric 1,6-conjugate addition of para-quinone methides (p-QMs), a class of challenging reactions with previous limited success. Benefiting from chiral Bronsted acid catalysis, which allows in situ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57f1c2d7e6a3b0a915cb4ec6bf0fe3f6
https://doi.org/10.1002/chin.201611055
https://doi.org/10.1002/chin.201611055
Publikováno v:
Angewandte Chemie (International ed. in English). 54(46)
Described herein is a general and mild catalytic asymmetric 1,6-conjugate addition of para-quinone methides (p-QMs), a class of challenging reactions with previous limited success. Benefiting from chiral Bronsted acid catalysis, which allows in situ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6e463a66643da0ccae4b6c66bcdbcee
https://pubmed.ncbi.nlm.nih.gov/26403542
https://pubmed.ncbi.nlm.nih.gov/26403542
Publikováno v:
Organic Letters; Oct2019, Vol. 21 Issue 19, p7746-7749, 4p