Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Guichun Fang"'
Publikováno v:
Chinese Journal of Chemistry. 41:1075-1079
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9deb8afda6e2ac7632fc583b113bc23
https://doi.org/10.1002/cjoc.202200713
https://doi.org/10.1002/cjoc.202200713
Autor:
Guichun Fang, Xihe Bi
Publikováno v:
Silver Catalysis in Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6260624f3c84ad0e69ed0938c3489942
https://doi.org/10.1002/9783527342822.ch11
https://doi.org/10.1002/9783527342822.ch11
Publikováno v:
Organic Letters. 20:7113-7116
An interrupted Schmidt rearrangement/Hosomi–Sakurai reaction of N-tosyl and S-substituted vinyl azides is reported. With BF3·Et2O as a Lewis acid promoter, the denitrogenative fragmentation of vinyl azides facilitates the generation of the N/S-sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b842300d9e30fe6242cbc2bcdc304157
https://doi.org/10.1021/acs.orglett.8b03062
https://doi.org/10.1021/acs.orglett.8b03062
Publikováno v:
Asian Journal of Organic Chemistry. 7:1066-1070
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9a8bbad2e89f7e3bac7bea2cc3ea37f
https://doi.org/10.1002/ajoc.201800172
https://doi.org/10.1002/ajoc.201800172
Publikováno v:
Advanced Synthesis & Catalysis. 359:1422-1502
Silver-mediated reactions have recently emerged as a frontier area in organic chemistry. Indeed, the remarkable property of silver as a single-electron oxidant has led to its exploitment into the field of radical chemistry. The excellent reactivity a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6f2db102fa1f96a47c23c0892209668
https://doi.org/10.1002/adsc.201601179
https://doi.org/10.1002/adsc.201601179
Publikováno v:
Organic Letters. 19:1346-1349
An unexpected silver-catalyzed cascade reaction of β-enaminones and isocyanoacetates affording functionalized pyrrole derivatives is reported. In this reaction, tautomeric equilibria of β-enaminones are utilized to generate imine partners in situ.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9103512e6d5c188f72110f60a5532d6a
https://doi.org/10.1021/acs.orglett.7b00201
https://doi.org/10.1021/acs.orglett.7b00201
Publikováno v:
Synthesis. 47:2317-2346
Propargylic alcohols, which possess inherent alkynyl and hydroxyl functional groups, are one of the most valuable bifunctional building blocks in the field of organic synthesis. The simple generation and conversion of these compounds into various val
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d05847aa19e557caa1403e50103e43fa
https://doi.org/10.1055/s-0034-1378852
https://doi.org/10.1055/s-0034-1378852
Publikováno v:
Organic Letters. 15:4126-4129
An atom-economic route to thiophenes and bithiophenes has been developed starting from the readily available gem-dialkylthio enynes. A range of functionalized thiophenes and bithiophenes, bearing a pendent vinylthio group, were obtained in good to hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f84ad3263e48ae17b0ec3a20061af42
https://doi.org/10.1021/ol4017854
https://doi.org/10.1021/ol4017854
Publikováno v:
RSC Adv.. 3:386-389
An unprecedented solvent-controlled, regio-switchable Knorr-type reaction for the synthesis of pyrazoles has been realized in the cyclocondensation of β-aminoenones with hydrazides. Single regioisomer of 3- or 5-arylaminopyrazole can be obtained sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7b3f5d57b88fd0373f4f0fe43f7a1c8
https://doi.org/10.1039/c2ra22647b
https://doi.org/10.1039/c2ra22647b
Publikováno v:
Chemistry, an Asian journal. 11(23)
An efficient Ag2CO3-promoted sulfonylation of allyl/propargyl alcohols with sodium sulfinates has been developed. The reaction tolerates a wide range of functional groups to deliver γ-keto sulfones in high yields (up to 93 %). Propargyl alcohols fur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d7dd1547ead44b9f6088c41f52b82ea
https://pubmed.ncbi.nlm.nih.gov/27860354
https://pubmed.ncbi.nlm.nih.gov/27860354