Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Enlu Ma"'
Publikováno v:
Energy & Fuels. 35:15770-15777
Lignin is a potential renewable raw material for synthesis of aromatic molecules and materials. Particularly, Kraft-type lignins are abundantly available as a byproduct of wood and paper industries. Currently, there are practically no valuable produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5a50411c5a348b7cb46cb47a8494c1c
https://doi.org/10.1021/acs.energyfuels.1c01968
https://doi.org/10.1021/acs.energyfuels.1c01968
The synthesis of new types of furan-based compounds other than 5-hydroxymethylfurfural from glucose is a very attractive yet underexploited strategy. We report here a catalytic conversion of glucose with acetylacetone (acac) to furan-centered chemica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdb5ba0a93ed3ebe9d4ab4fa04e78a24
http://hdl.handle.net/10138/333262
http://hdl.handle.net/10138/333262
Publikováno v:
Asian Journal of Organic Chemistry. 8:1834-1837
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edcd1c01ccbff5bda365b33ca151e694
https://doi.org/10.1002/ajoc.201900409
https://doi.org/10.1002/ajoc.201900409
Publikováno v:
Asian Journal of Organic Chemistry. 7:914-917
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e7eeb9e11019617df848dee78607d7a
https://doi.org/10.1002/ajoc.201800057
https://doi.org/10.1002/ajoc.201800057
Publikováno v:
Angewandte Chemie. 128:10566-10569
Exploiting catalytic carbonyl-olefin metathesis is an ongoing challenge in organic synthesis. Reported herein is an FeCl3 -catalyzed ring-closing carbonyl-olefin metathesis. The protocol allows access to a range of carbo-/heterocyclic alkenes with go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ca924fe8635e572fef670d9ae6f2b8b
https://doi.org/10.1002/ange.201604349
https://doi.org/10.1002/ange.201604349
Publikováno v:
Tetrahedron. 72:4111-4116
Catalyst-controlled divergent reactions of thiophenols with alkenes bearing heteroatoms have been developed. Markovnikov-type hydrothiolation products and thioacetals were synthesized selectively by switching copper catalysts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::074115ad57bf98b19947b7f49b459b19
https://doi.org/10.1016/j.tet.2016.05.050
https://doi.org/10.1016/j.tet.2016.05.050
Publikováno v:
Tetrahedron Letters. 57:2211-2214
Iron-catalyzed allylic substitution of allylic ethers with Grignard reagents is reported. Phenoxy group is successfully applied as a leaving group in iron-catalyzed allylic substitution reactions with Grignard reagents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6885c640344565aa8f9ed08897b74ca1
https://doi.org/10.1016/j.tetlet.2016.04.027
https://doi.org/10.1016/j.tetlet.2016.04.027
Publikováno v:
ChemInform. 47
Exploiting catalytic carbonyl-olefin metathesis is an ongoing challenge in organic synthesis. Reported herein is an FeCl3 -catalyzed ring-closing carbonyl-olefin metathesis. The protocol allows access to a range of carbo-/heterocyclic alkenes with go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de58ea56b67aba6b3c62ec30b65f18d8
https://doi.org/10.1002/chin.201652055
https://doi.org/10.1002/chin.201652055
Publikováno v:
ChemInform. 47
Catalyst-controlled divergent reactions of thiophenols with alkenes bearing heteroatoms have been developed. Markovnikov-type hydrothiolation products and thioacetals were synthesized selectively by switching copper catalysts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbb80b5020fd342a578144f6ed337a6d
https://doi.org/10.1002/chin.201643086
https://doi.org/10.1002/chin.201643086
Publikováno v:
ChemInform. 47
Iron-catalyzed allylic substitution of allylic ethers with Grignard reagents is reported. Phenoxy group is successfully applied as a leaving group in iron-catalyzed allylic substitution reactions with Grignard reagents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cd6090dee2a32dd332a85b1fc9732c4
https://doi.org/10.1002/chin.201635028
https://doi.org/10.1002/chin.201635028