Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Yongliang Tu"'
Publikováno v:
Advanced Synthesis & Catalysis. 5/23/2023, Vol. 365 Issue 10, p1613-1617. 5p.
Publikováno v:
Advanced Synthesis & Catalysis. 364:1522-1525
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e943d4f6cc689823da54d7d5d443444b
https://doi.org/10.1002/adsc.202200190
https://doi.org/10.1002/adsc.202200190
Publikováno v:
Organic Letters. 24:2238-2241
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de5102fe2308d043a8c7f400e96d0fed
https://doi.org/10.1021/acs.orglett.2c00622
https://doi.org/10.1021/acs.orglett.2c00622
Publikováno v:
The Journal of Organic Chemistry. 87:3817-3824
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0d2af9d21a356d99090f444d8ad3048
https://doi.org/10.1021/acs.joc.1c02971
https://doi.org/10.1021/acs.joc.1c02971
Autor:
Yongliang Tu, Junfeng Zhao
Publikováno v:
The Chemical Record. 21:3442-3457
Both arylhydrazines and quaternary ammonium salts are readily accessible or commercially available chemicals that show versatile reactivity in Pd-catalyzed coupling reactions via C-N bond cleavage. A tremendous array of coupling reactions involving r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1baf2c6797f4af27a37770d3b1aab10
https://doi.org/10.1002/tcr.202100089
https://doi.org/10.1002/tcr.202100089
Publikováno v:
Advanced Synthesis & Catalysis. 363:1330-1334
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::570dd463823f8fb142e940daa481ca02
https://doi.org/10.1002/adsc.202001440
https://doi.org/10.1002/adsc.202001440
Publikováno v:
Angewandte Chemie (International ed. in English). 61(30)
In a ball mill, FeBr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51ea0b6d239d9a9639ad3cd6ced64783
https://pubmed.ncbi.nlm.nih.gov/35511087
https://pubmed.ncbi.nlm.nih.gov/35511087
Publikováno v:
Organic Letters. 22:8842-8845
A rhodium-catalyzed C-H amidation/cyclization sequence provides benzothiadiazine-1-oxides from sulfoximines and 1,4,2-dioxazol-5-ones in good yields. The reaction is characterized by a high functional group tolerance and, in contrast to most previous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25fd5e1422a36b02058cfa3fd6579911
https://doi.org/10.1021/acs.orglett.0c03212
https://doi.org/10.1021/acs.orglett.0c03212
Publikováno v:
Organic Letters. 22:8937-8940
In visible light, sulfoximidoyl-containing hypervalent iodine reagents react with aryl alkynes to give N-α-ketoacylated sulfoximines in good to high yields. The process is metal- and base-free, pro...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d648c9fa443f1739ad1ef3594b10c10e
https://doi.org/10.1021/acs.orglett.0c03338
https://doi.org/10.1021/acs.orglett.0c03338
Publikováno v:
The Journal of Organic Chemistry. 85:5245-5254
An efficient base-promoted tandem reaction between vinyl 1,1-dichlorides and secondary sulfonamides with ynamide as the key intermediate is described. This method provides a facile approach to (Z)-1,2-endiamide and aryl 1,1-endiamide derivatives via
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ff74b68bb5ee81349ee26e7a99e405c
https://doi.org/10.1021/acs.joc.9b03305
https://doi.org/10.1021/acs.joc.9b03305