Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vasily A. Ignatenko"'
Publikováno v:
The Journal of Organic Chemistry. 78:3821-3831
Triterpenoids comprise a very diverse family of polycyclic molecules that is well-known to possess a myriad of medicinal properties. Therefore, triterpenoids constitute an attractive target for medicinal chemistry and diversity-oriented synthesis. Ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ee7a2e73d2b4fdeda0957f743e922dd
https://doi.org/10.1021/jo400275p
https://doi.org/10.1021/jo400275p
Publikováno v:
Tetrahedron Letters. 52:1269-1272
A concise and practical strategy to obtain C3 reverse-prenylated pyrrolidinoindoline scaffold has been executed in 28.8% overall yield. The key conjugative step involved a Booker-Milburn–Feudoloff reaction involving an NCS-mediated activation of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c49f3fbdeabb2c4a917b232713d58d2c
https://doi.org/10.1016/j.tetlet.2011.01.020
https://doi.org/10.1016/j.tetlet.2011.01.020
Publikováno v:
The Journal of organic chemistry. 78(23)
In an effort to access biologically relevant chemical space, a complex natural product-derived non-symmetrical diketone was prepared as a substrate for divergent transannular aldol reactions. The use of common aldol conditions resulted in predominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d463b5705cc7d31b9c4f3dfc25dbebd6
https://pubmed.ncbi.nlm.nih.gov/24161022
https://pubmed.ncbi.nlm.nih.gov/24161022
Publikováno v:
The Journal of organic chemistry. 78(2)
The remodeling of a natural product core framework by means of diversity-oriented synthesis (DOS) is a valuable approach to access diverse/biologically relevant chemical space and to overcome the limitations of combinatorial-type compounds. Here we p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb115e95fce1fd49d724c65dfceb18c3
https://pubmed.ncbi.nlm.nih.gov/23245400
https://pubmed.ncbi.nlm.nih.gov/23245400
Publikováno v:
ChemInform. 41
In the presence of PdCl2(PPh3)2 amides of type (IV) undergo a novel cyclization to 2,2-dimethyl indenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae79c3853e90b663ffcf0fdd021698a7
https://doi.org/10.1002/chin.201050115
https://doi.org/10.1002/chin.201050115
Publikováno v:
Organic letters. 12(16)
In an effort to access biologically important scaffolds, a concise branch-selective synthesis of C3 tertiary oxindoles by Cu(I)-catalyzed aryl amidation and 2,2-dimethyl indene by Pd(0)-catalyzed Heck cyclization has been accomplished from acyclic re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e91ee62697d9adbb850e9c0695fc30bd
https://pubmed.ncbi.nlm.nih.gov/20704399
https://pubmed.ncbi.nlm.nih.gov/20704399
Publikováno v:
Organic Letters; Aug2010, Vol. 12 Issue 16, p3594-3597, 4p