Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Cheng‐Tao Feng"'
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 7, Pp o2021-o2021 (2012)
In the title compound, C21H19NO2, the six-membered heterocycle assumes a screw-boat conformation. The phenyl ring is oriented with respect to the pyrrole ring at a dihedral angle of 64.76 (10)°. An intramolecular C—H...O hydrogen bond helps to sta
Externí odkaz:
https://doaj.org/article/448af4c2e6d54a92ad29362b04ea78b6
Publikováno v:
Advanced Synthesis & Catalysis. 365:871-876
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::355a30acdcfd3dbc50969fba2b9e8236
https://doi.org/10.1002/adsc.202201361
https://doi.org/10.1002/adsc.202201361
Publikováno v:
Combinatorial Chemistry & High Throughput Screening. 24:1114-1125
Background: Buyang Huanwu Tang (BYHWT) and relevant Traditional Chinese medicine (TCM) has its unique advantages in the treatment of cerebral ischemia. However, its pharmacological mechanism has not been fully explained. Objective: Base on the multi-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c22ec7f9c96b272c504b1732ea5aac09
https://doi.org/10.2174/1386207323666200901100529
https://doi.org/10.2174/1386207323666200901100529
Publikováno v:
The European Physical Journal Special Topics. 230:1989-1997
Neurons can exhibit abundant electrical activities in response to various externally applied stimuli, which can lay the groundwork for widening their use in neuron-based engineering applications. This paper presents the dynamical behaviors and analog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06742258268eb106fa09a9ba83b25b84
https://doi.org/10.1140/epjs/s11734-021-00183-0
https://doi.org/10.1140/epjs/s11734-021-00183-0
Publikováno v:
Organic Letters. 23:4214-4218
An electrochemically regioselective C-H phosphorothiolation of (hetero)arenes with thiocyanate as the S source under ultrasonic irradiation has been developed. The synergistic cooperation of electrooxidation and ultrasonication markedly accelerated t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b757e507056d12f57025e7d19b3c20e6
https://doi.org/10.1021/acs.orglett.1c01161
https://doi.org/10.1021/acs.orglett.1c01161
Publikováno v:
Organic Chemistry Frontiers. 8:6384-6389
An I2O5 promoted tandem Strecker/C(sp3)–H amination reaction of pyridine-2-carboxaldehydes, benzylamines and NH4SCN has been reported. This multicomponent reaction that allows the single-step construction of biologically important cyano-functionali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53d392b3624ad288cd1603e9d5e2ecb0
https://doi.org/10.1039/d1qo01060c
https://doi.org/10.1039/d1qo01060c
Publikováno v:
Chemical Communications. 57:5338-5341
A NaI-promoted sequential double carbon-sulfur bond formation was developed to afford sulfur-bridged imidazopyridines, using Deoxofluor as the sulfur source and requiring only 15 min at room temperature. Using this process, imidazo[1,5-a]pyridines co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::587f1d9ddd683bb06c775b7497e63337
https://doi.org/10.1039/d1cc01044a
https://doi.org/10.1039/d1cc01044a
Publikováno v:
Organic & Biomolecular Chemistry. 17:6570-6573
The ring-opening reaction of imidazo[1,5-a]quinolines under photoredox conditions has been described. With Eosin Y as the organophotoredox catalyst, synthetically useful and medicinally important imides were obtained in moderate to excellent yields u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fce2834ec3d2dc125e85ed61321093c6
https://doi.org/10.1039/c9ob01227c
https://doi.org/10.1039/c9ob01227c
Publikováno v:
Current pharmaceutical biotechnology. 23(3)
Background: Quercitrin is widely found in herbal medicines, and it is particularly important in the design of new therapeutic agents. Because of its wide range of biological activities, methods for detecting quercitrin and its pharmacokinetics in bio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6df028beffc879a56c7ca24c97c8893
https://pubmed.ncbi.nlm.nih.gov/34011255
https://pubmed.ncbi.nlm.nih.gov/34011255
Publikováno v:
Advanced Synthesis & Catalysis. 360:4726-4730
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e224eb3a5fd623741b0e55f1bb9a876b
https://doi.org/10.1002/adsc.201801060
https://doi.org/10.1002/adsc.201801060