Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tengwei Xu"'
Publikováno v:
Synlett. 31:363-368
A visible-light-induced direct C–H alkylation of imidazo[1,2-a]pyridines has been developed. It proceeds at room temperature by employing inexpensive Eosin Y as a photocatalyst and alkyl N-hydroxyphthalimide (NHP) esters as alkylation reagents. A v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::973f32720430430a8540136dbe573c1c
https://doi.org/10.1055/s-0039-1691567
https://doi.org/10.1055/s-0039-1691567
Publikováno v:
Organic Chemistry Frontiers. 7:113-118
A novel avenue of C–CN bond construction was facilely achieved via the TBHP-mediated oxidative coupling reaction between quinoxalin-2(1H)-one derivatives and ammonium thiocyanate without any metal catalyst. Applying this protocol, a variety of 3-cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1c67de4a64814f84fe8cc76ec72cd06
https://doi.org/10.1039/c9qo01055f
https://doi.org/10.1039/c9qo01055f
Autor:
Xiaohui Zhuang, Bin Sun, Liang Zhang, Rui Zhu, Rongcheng Shi, Jin Yang, Xun Zhang, Chuanming Yu, Tengwei Xu, Can Jin
Publikováno v:
Asian Journal of Organic Chemistry. 8:2058-2064
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7584b20c74542407f4ccc7636a55bcae
https://doi.org/10.1002/ajoc.201900542
https://doi.org/10.1002/ajoc.201900542
Publikováno v:
Asian Journal of Organic Chemistry. 8:1942-1946
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c111b00c4e50b730f23e99b7bc3de0ee
https://doi.org/10.1002/ajoc.201900414
https://doi.org/10.1002/ajoc.201900414
Publikováno v:
Synlett. 30:1585-1591
A facile iron-catalyzed decarboxylative radical coupling of alkyl diacyl peroxides with coumarins or chromones has been developed, affording a highly efficient approach to synthesize a variety of α-alkylated coumarins and β-alkylated chromones. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bca373a96ee7d7c0e5c321eb2d7edd8
https://doi.org/10.1055/s-0037-1611864
https://doi.org/10.1055/s-0037-1611864
A Facile Synthesis of 3β,25-dihydroxy-5α-Cholest-7-ene, the Precursor to HMG-CoA Reductase Inhibitor
Publikováno v:
Journal of Chemical Research. 42:156-159
An efficient four-step procedure is described for the synthesis of 3β,25-dihydroxy-5α-cholest-7-ene from 3β-hydroxy-5α-cholesta-7,24-diene in an overall yield of 34%. This product can serve as a precursor for the synthesis of an inhibitor of 3-hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5df53d1713cc19dc0272ad4cb32a353
https://doi.org/10.3184/174751918x15220628915420
https://doi.org/10.3184/174751918x15220628915420
A facile synthesis of 3β,25-dihydroxy-5α-cholest-7-ene, the precursor to HMGCoA reductase inhibitor.
Publikováno v:
Journal of Chemical Research; 2018 Supplement 3, Vol. 42, p156-156, 1/2p