Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Gavin Chit Tsui"'
Publikováno v:
Organic Letters. 25:2333-2337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d732afa89f2896772fb8b12509328f8
https://doi.org/10.1021/acs.orglett.3c00718
https://doi.org/10.1021/acs.orglett.3c00718
Publikováno v:
Organic Letters. 25:1088-1093
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dedb44f7238f5196fcddf5ebf167ccd9
https://doi.org/10.1021/acs.orglett.2c04315
https://doi.org/10.1021/acs.orglett.2c04315
Publikováno v:
Organic Letters. 25:877-882
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1670c9c416cc89c81bc179577c65478
https://doi.org/10.1021/acs.orglett.3c00108
https://doi.org/10.1021/acs.orglett.3c00108
Publikováno v:
Organic Letters. 24:4087-4092
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc09ac75e347652e69664090c4b0e4e8
https://doi.org/10.1021/acs.orglett.2c01639
https://doi.org/10.1021/acs.orglett.2c01639
Autor:
Ziwei Luo, Gavin Chit Tsui
Publikováno v:
Organic Chemistry Frontiers. 9:4969-4974
A domino radical cyclization/bis(pentafluoroethylation) of 1,6-dienes is described. This method provides access to N-heterocycles/carbocycles containing two C2F5 groups in one step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d56b5691790f3af78dec0741f33f6ed6
https://doi.org/10.1039/d2qo00919f
https://doi.org/10.1039/d2qo00919f
Autor:
Ren-Xiao Liang, Jian-Fei Chen, Ying-Ying Huang, Ya-Ping Yu, Han-Yue Zhang, Yu-Feng Song, Gavin Chit Tsui, Yi-Xia Jia
Publikováno v:
Chemical Communications. 58:6200-6203
Highly enantioselective palladium-catalyzed dearomative reductive Heck and domino Heck–Suzuki reactions of 2-CF3-indoles have been developed towards the synthesis of indolines bearing trifluoromethyl quaternary stereocenters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e7feb354df701b84cdc232fd339dedc
https://doi.org/10.1039/d2cc01435a
https://doi.org/10.1039/d2cc01435a
Autor:
Xinkan Yang, Gavin Chit Tsui
Publikováno v:
Synlett. 33:713-720
Organic molecules containing the trifluoromethyl (CF3) group play a vital role in pharmaceuticals, agrochemicals, and materials. New trifluoromethylation methods should encompass capabilities to address issues in efficiency, selectivity, and CF3 sour
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3dc96b25b29d0aec8de4665e11b7928
https://doi.org/10.1055/a-1709-3098
https://doi.org/10.1055/a-1709-3098
Publikováno v:
Organic Letters. 23:8072-8076
We herein describe a Pd-catalyzed stereoselective C-F bond vinylation and allylation reaction of tetrasubstituted gem-difluoroalkenes for the synthesis of valuable monofluorinated 1,3- and 1,4-dienes with excellent diastereoselectivities. Different f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd7ed432fcd73bb0984f6e08e0718516
https://doi.org/10.1021/acs.orglett.1c03096
https://doi.org/10.1021/acs.orglett.1c03096
Publikováno v:
Organic Letters. 23:6169-6173
We herein describe a nucleophilic vinylic substitution (SNV) of trisubstituted monofluoroalkenes with excellent stereocontrol (d.r. > 99:1). Starting from (E)-β-monofluoroacrylates, various trisubstituted (E)-alkenes containing O/N/S-substituent gro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfbbbed7e96a156846058fa96f3fa3db
https://doi.org/10.1021/acs.orglett.1c02359
https://doi.org/10.1021/acs.orglett.1c02359
Publikováno v:
Organic Letters. 23:5241-5245
A highly diastereoselective Pd(0)-catalyzed synthesis of difluorinated 1,3-dienes is described. Symmetrical 1,3-dienes containing a vicinal difluoro moiety can be obtained as single diastereomers from tetrasubstituted gem-difluoroalkenes. The reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00db1cdea63de7ff4ebc9b48a5363a17
https://doi.org/10.1021/acs.orglett.1c01768
https://doi.org/10.1021/acs.orglett.1c01768