Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rong-Ye Zhou"'
Publikováno v:
Organic Preparations and Procedures International. 53:397-401
Idebenone (Figure 1) is a synthetic analogue of Coenzyme Q10 (CoQ10),1 which functions as an antioxidant and free radical scavenging molecule. Structurally, idebenone and CoQ10 share the same 1,4-b...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fab227b98d3d3b1eed861a57a4ef7411
https://doi.org/10.1080/00304948.2021.1917945
https://doi.org/10.1080/00304948.2021.1917945
Publikováno v:
The Journal of Organic Chemistry. 85:10973-10979
PGL-1 epitope 1 bearing a p-aminoethylphenol group was efficiently synthesized by using linear synthetic routes. A method for efficient synthesis of oligosaccharides containing rhamnose rings was developed. The chemistry is flexible and could be used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e305d797ef119d80609e38a4ccaacb6
https://doi.org/10.1021/acs.joc.0c01088
https://doi.org/10.1021/acs.joc.0c01088
Publikováno v:
Chemical Communications. 56:14067-14070
Non-natural PIM epitope Ac2PIM2 was presented by CD1b to active T cell to release IFN-γ.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92fc8adbca44cc97c1f939a008899aa5
https://doi.org/10.1039/d0cc05573e
https://doi.org/10.1039/d0cc05573e
Publikováno v:
New Journal of Chemistry. 47:515-515
Correction for ‘AgNO3-catalyzed decarboxylative cross-coupling reaction: an approach to coenzyme Q’ by Wan-Yue Luo et al., New J. Chem., 2020, 44, 8702–8704, https://doi.org/10.1039/D0NJ01497D.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f73f1c44a689347c4577a919b6b229d2
https://doi.org/10.1039/d2nj90168d
https://doi.org/10.1039/d2nj90168d
Publikováno v:
Chemical communications (Cambridge, England). 57(48)
Retraction of 'Chemical synthesis and antigenic activity of a phosphatidylinositol mannoside epitope from Mycobacterium tuberculosis' by Shi-Yuan Zhao et al., Chem. Commun., 2020, 56, 14067-14070, DOI: 10.1039/D0CC05573E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5c9657fb4183d13bba8b09412b26ef80
https://pubmed.ncbi.nlm.nih.gov/33104149
https://pubmed.ncbi.nlm.nih.gov/33104149
Publikováno v:
New Journal of Chemistry. 44:8702-8704
An efficient and general method for the synthesis of coenzyme Q compounds through the activation of the 1,4-benzoquinone Csp2–H bond has been developed. This C–C bond formation reaction proceeds readily in an open flask by the direct cross-coupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::552ef63e43d3fa17794b5de3bcdb536a
https://doi.org/10.1039/d0nj01497d
https://doi.org/10.1039/d0nj01497d
Publikováno v:
Chemical communications (Cambridge, England). 56(90)
Phosphatidylinositol mannosides (PIMs) have been investigated as lipidic antigens for a new subunit tuberculosis vaccine. A non-natural diacylated phosphatidylinositol mannoside (Ac2PIM2) was designed and synthesized by mimicking the natural PIM6 pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5657510c34021c910461ffd147c295ec
https://pubmed.ncbi.nlm.nih.gov/34095918
https://pubmed.ncbi.nlm.nih.gov/34095918
Publikováno v:
The Journal of organic chemistry. 85(16)
PGL-1 epitope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::75c0a6aecd4b05dd7950e8d7949c32dd
https://pubmed.ncbi.nlm.nih.gov/34003653
https://pubmed.ncbi.nlm.nih.gov/34003653
Publikováno v:
The Journal of Organic Chemistry. 86:7891-7891
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb19aab120300077836daffc9fbd9188
https://doi.org/10.1021/acs.joc.1c00934
https://doi.org/10.1021/acs.joc.1c00934
Publikováno v:
Chemical Communications. 57:5985-5985
Retraction of ‘Chemical synthesis and antigenic activity of a phosphatidylinositol mannoside epitope from Mycobacterium tuberculosis’ by Shi-Yuan Zhao et al., Chem. Commun., 2020, 56, 14067–14070, DOI: 10.1039/D0CC05573E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf910f08fbb789dfe2ce003b7b7f0e9a
https://doi.org/10.1039/d1cc90195h
https://doi.org/10.1039/d1cc90195h