Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Wen-Xue Huang"'
Autor:
Jun-Ying Wang, Wen-Xue Huang, Yu-Lin Tian, Yong-Sheng Wang, Yue Wang, Wan-Li Zhang, Yuan-Jun Huang, Zai-Guo Gan, Hu-Shan Xu
Publikováno v:
Atoms, Vol 11, Iss 11, p 139 (2023)
To precisely measure atomic masses and select neutron-deficient isotopes produced by fusion evaporation reactions, an MRTOF-MS (multi-reflection time-of-flight mass spectrometer) at the SHANS (Spectrometer for Heavy Atom and Nuclear Structure) is bei
Externí odkaz:
https://doaj.org/article/37a8771c8b554b8c914123e5fef769c7
Autor:
Wen-Xue Huang, Yong-Sheng Wang, Yu-Lin Tian, Jun-Ying Wang, Yue Wang, Zai-Guo Gan, Hu-Shan Xu
Publikováno v:
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment. 1047:167825
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::912020f8f8d2e26a8fa85451cea8514f
https://doi.org/10.1016/j.nima.2022.167825
https://doi.org/10.1016/j.nima.2022.167825
Publikováno v:
ACS Catalysis. 6:2368-2371
A highly enantioselective hydrogenation of heteroaromatics bearing a hydroxyl group, 3-hydroxypyridinium salts, has been successfully developed using chiral iridium catalyst, providing a direct access to trans 6-substituted piperidin-3-ols with up to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::554752550f71dd377071a06f5200ab25
https://doi.org/10.1021/acscatal.5b02625
https://doi.org/10.1021/acscatal.5b02625
Publikováno v:
Angewandte Chemie. 127:12124-12128
Ap alladium-catalyzed enantioselective C¢ Hf unc- tionalization of indoles was achieved with an axially chiral 2,2'- bipyridine ligand, thus providing the desired indol-3-acetate derivatives with up to 98 %e e. Moreover ,t he reaction protocol was a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd9650ac41e09fabc2ec0e75d7f4a88
https://doi.org/10.1002/ange.201504483
https://doi.org/10.1002/ange.201504483
Publikováno v:
Tetrahedron Letters. 56:4334-4338
An efficient bifunctional squaramide-catalyzed Michael addition/cyclization reaction of o-quinone methides generated in situ from 2-(1-tosylalkyl)phenols with active methylene compounds bearing a cyano group has been realized to synthesize chiral 2-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e9263b1680cef9236e7e04dcaf6a68d
https://doi.org/10.1016/j.tetlet.2015.05.076
https://doi.org/10.1016/j.tetlet.2015.05.076
Publikováno v:
Journal of the American Chemical Society. 136:15837-15840
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate generated in situ from acid-catalyzed aza-Pinacol rearrangement has been successfully developed, providing efficient access to chiral exocyclic amines wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c7b243e4f6b9a1a3d5e67bb3050ff0d
https://doi.org/10.1021/ja5075745
https://doi.org/10.1021/ja5075745
Publikováno v:
Organic Letters. 16:3324-3327
Highly enantioselective iridium-catalyzed hydrogenation of pyrrolo[1,2-a]pyrazinium salts has been achieved, providing a direct access to chiral 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine derivatives with up to 95% ee. The key feature of the reaction i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa1c24727beeb68246386fb68048805
https://doi.org/10.1021/ol5013313
https://doi.org/10.1021/ol5013313
Publikováno v:
ChemInform. 47
A facile method has been developed for the synthesis of chiral piperazines through Ir-catalyzed hydrogenation of pyrazines activated by alkyl halides, giving a wide range of chiral piperazines including 3-substituted as well as 2,3- and 3,5-disubstit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1f735381a4b226f9e3c5eb95a27c454
https://doi.org/10.1002/chin.201649173
https://doi.org/10.1002/chin.201649173
Publikováno v:
Organic letters. 18(13)
A facile method has been developed for the synthesis of chiral piperazines through Ir-catalyzed hydrogenation of pyrazines activated by alkyl halides, giving a wide range of chiral piperazines including 3-substituted as well as 2,3- and 3,5-disubstit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba7c26f3b5fae40193eb9d9faf3e0a8a
https://pubmed.ncbi.nlm.nih.gov/27295391
https://pubmed.ncbi.nlm.nih.gov/27295391
Publikováno v:
ChemInform. 47
Ap alladium-catalyzed enantioselective C¢ Hf unc- tionalization of indoles was achieved with an axially chiral 2,2'- bipyridine ligand, thus providing the desired indol-3-acetate derivatives with up to 98 %e e. Moreover ,t he reaction protocol was a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b3c9417843becb58370eaf2a921c1e4
https://doi.org/10.1002/chin.201607138
https://doi.org/10.1002/chin.201607138