Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Zhenjun Mao"'
The health of people is seriously threatened by the class of disorders known as tumors because of their high risk and high mortality. Early detection and treatment are the most efficient approaches to stop cancers and lower mortality, according to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a0bbabda239f2cb9d05f5c83a25ce51
https://doi.org/10.21203/rs.3.rs-2639685/v1
https://doi.org/10.21203/rs.3.rs-2639685/v1
Autor:
Zhenjun Mao, Hao Zeng
Publikováno v:
RSC advances. 12(38)
A gold-catalyzed regioselective [3 + 2] cycloaddition of alkynyl triazenes with 1,2,4-dioxazoles was developed. The triazene group in the products could be replaced to obtain iodo-oxazoles, providing potential transformations to diverse oxazole struc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba27abb34140a608c20bb1c460956e2d
https://pubmed.ncbi.nlm.nih.gov/36128381
https://pubmed.ncbi.nlm.nih.gov/36128381
Publikováno v:
Catalysts, Vol 11, Iss 1078, p 1078 (2021)
The Pd/C-catalyzed reactions, including reduction reactions and cross-coupling reactions, play an irreplaceable role in modern organic synthesis. Compared to the homogeneous palladium catalyst system, the heterogeneous Pd/C catalyst system offers an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::241814b7777f96843416aaef219029e1
https://www.mdpi.com/2073-4344/11/9/1078
https://www.mdpi.com/2073-4344/11/9/1078
Publikováno v:
Daxue Huaxue. :2109076
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ef34f745ef231e11cce87d78a0b840d
https://doi.org/10.3866/pku.dxhx202109076
https://doi.org/10.3866/pku.dxhx202109076
Publikováno v:
Organic Letters. 18:4888-4891
The para-quinone methides (p-QMs) are activated by Lewis acid and then attacked by diazo compounds. The following rearrangement leads to nitrogen gas extrusion and C–C double bond formation to constitute a metathesis reaction process. Therefore, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d444ee464798da608073f2bfe2c4e1f0
https://doi.org/10.1021/acs.orglett.6b02365
https://doi.org/10.1021/acs.orglett.6b02365
Publikováno v:
Organic Letters. 18:2722-2725
A novel Fe-catalyzed hydroalkylation of olefins with para-quinone methides (p-QMs) for accessing phenols has been developed. In this protocol, various olefins could convert to alkyl radicals and undergo addition to para-quinone methides toward C-C bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58e2ac406ea4b14ecad7e3238fe51c1f
https://doi.org/10.1021/acs.orglett.6b01173
https://doi.org/10.1021/acs.orglett.6b01173
Publikováno v:
Organic & Biomolecular Chemistry. 14:6201-6204
A Rh(iii)-catalyzed C-H activation/cyclization of oximes and alkenes for facile and regioselective access to isoquinolines has been developed. This protocol features mild reaction conditions and easily accessible starting materials, and has been appl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d468003f4aac438836dc2ae055be33af
https://doi.org/10.1039/c6ob00942e
https://doi.org/10.1039/c6ob00942e
Publikováno v:
Synlett. 27:546-550
An efficient binary acid catalyzed asymmetric intramolecular tandem 1,5-hydride transfer/ring-closure reaction was achieved. The process is catalyzed by the combination of a chiral spirocyclic phosphoric acid and magnesium chloride to afford struct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eac3ab7d15362814599197fbeec8b23b
https://doi.org/10.1055/s-0035-1560198
https://doi.org/10.1055/s-0035-1560198
Publikováno v:
Chemistry - A European Journal. 21:9039-9043
Highly efficient synthesis of optically enriched pyrrolobenzo-1,4-diazines bearing quaternary stereocenters has been realized through the chiral Brønsted acid-catalyzed Pictet-Spengler reaction of 2-(1H-pyrrol-1-yl)anilines and α-ketoamides in good
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91a6a7004e95c9320bf1e37c7ab37576
https://doi.org/10.1002/chem.201500823
https://doi.org/10.1002/chem.201500823
Publikováno v:
ChemInform. 47
A Rh(III)-catalyzed C–H activation/cyclization of oximes and alkenes for facile and regioselective access to isoquinolines has been developed. This protocol features mild reaction conditions and easily accessible starting materials, and has been ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f92666f583a8dc3ef2a223c39c18d9f4
https://doi.org/10.1002/chin.201646165
https://doi.org/10.1002/chin.201646165