Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mastaneh Safarnejad Shad"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2142-2155 (2019)
In this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known “click reaction” (
Externí odkaz:
https://doaj.org/article/85f460a67e374a9299233f6f79c04f07
Autor:
Mastaneh Safarnejad Shad, Sandra Claes, Eline Goffin, Tom Van Loy, Dominique Schols, Steven De Jonghe, Wim Dehaen
Publikováno v:
Molecules, Vol 26, Iss 20, p 6297 (2021)
An expansion of the structure–activity relationship study of CXCR4 antagonists led to the synthesis of a series of isoquinolines, bearing a tetrahydroquinoline or a 3-methylpyridinyl moiety as head group. All compounds were investigated for CXCR4 a
Externí odkaz:
https://doaj.org/article/987ef9297c144093a160c41d8fc60881
Autor:
Mastaneh Safarnejad Shad, S. S. Zhokhov, Victor B. Rybakov, Maksim А. Boichenko, Olga A. Ivanova, Konstantin V. Anisovich, Igor V. Truhskov, Wim Dehaen
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:817-822
The intramolecular oxidative coupling of electron-rich aromatic groups in 5-(het)aryl-1-(het)arylalkyl-1 H -1,2,3-triazoles was studied in detail. Under treatment with phenyliodoso bis(trifluoroacetate) and boron trifluoride etherate these substrates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5af1d58f322fa9c2417f1f116b93a125
https://doi.org/10.1007/s10593-021-02985-5
https://doi.org/10.1007/s10593-021-02985-5
Autor:
Dominique Schols, Sandra Claes, Wim Dehaen, Mastaneh Safarnejad Shad, Eline Goffin, Steven De Jonghe, Tom Van Loy
Publikováno v:
Molecules; Volume 26; Issue 20; Pages: 6297
Molecules, Vol 26, Iss 6297, p 6297 (2021)
Molecules
Molecules, Vol 26, Iss 6297, p 6297 (2021)
Molecules
An expansion of the structure-activity relationship study of CXCR4 antagonists led to the synthesis of a series of isoquinolines, bearing a tetrahydroquinoline or a 3-methylpyridinyl moiety as head group. All compounds were investigated for CXCR4 aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e38b113b8bd97240df350f607af35146
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2142-2155 (2019)
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2142-2155 (2019)
In this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known "click reaction" (CuAA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9947dd800809c2d519ce63f1dccf09c
https://doi.org/10.3762/bjoc.15.211
https://doi.org/10.3762/bjoc.15.211