Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mitko Miliovsky"'
Autor:
Mitko Miliovsky, Ivan Svinyarov, Elena Prokopova, Daniela Batovska, Simeon Stoyanov, Milen G. Bogdanov
Publikováno v:
Molecules, Vol 20, Iss 2, Pp 2555-2575 (2015)
A series of sixteen polyhydroxylated trans-restricted 2-arylcinnamic acid analogues 3a–p were synthesized through a one-pot reaction between homophthalic anhydrides and various aromatic aldehydes, followed by treatment with BBr3. The structure of t
Externí odkaz:
https://doaj.org/article/3c5b55c3d227410ba1c2025500211bb7
Autor:
Maya Chochkova, Dilyana Nikolova, Yavor Mitrev, Mitko Miliovsky, Ivan Svinyarov, Yana Evstatieva, Milen G. Bogdanov
Publikováno v:
ChemInform. 44
The title compounds are tested as radical scavenger, antifungal agents, and tyrosinase inhibitors.
Autor:
Dilyana Nikolova, Ivan Svinyarov, Yavor Mitrev, Mitko Miliovsky, Yana Evstatieva, Maya Chochkova, Milen G. Bogdanov
A series of new stilbenes 4a–e, 5 were synthesized through a novel one-pot Perkin-like reaction between 6,7-dimethoxyhomophthalic anhydride and aromatic aldehydes, followed by treatment with BBr3. This synthesis is straightforward and allows polyhy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bef51b5a388aa3a6a2bb1c8c9188bd78
Autor:
Elena Prokopova, Milen G. Bogdanov, Ivan Svinyarov, Mitko Miliovsky, Daniela I. Batovska, Simeon Stoyanov
Publikováno v:
Molecules
Molecules, Vol 20, Iss 2, Pp 2555-2575 (2015)
Volume 20
Issue 2
Pages 2555-2575
Molecules, Vol 20, Iss 2, Pp 2555-2575 (2015)
Volume 20
Issue 2
Pages 2555-2575
A series of sixteen polyhydroxylated trans-restricted 2-arylcinnamic acid analogues 3a–p were synthesized through a one-pot reaction between homophthalic anhydrides and various aromatic aldehydes, followed by treatment with BBr3. The structure of t