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Akademický článek

Autor: V. Kovacik, M. Ruzinsky, J. Zaletova, P. Kutschy, M. Dzurilla

Publikováno v: Molecules, Vol 6, Iss 9, Pp 716-720 (2001)

In this paper we describe a new method for the synthesis of camalexin (1) based on the reaction of 1-(tert-butoxycarbonyl)indole-3-carboxaldehyde with methyl Lcysteinate hydrochloride, followed by oxidation and decarboxylation. Compounds 1, and inter

Externí odkaz: https://doaj.org/article/ee6f361518d64b809f201d31a046525b

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Akademický článek

Synthesis and antiproliferative activity of 1-methoxy-, 1-(α-D-ribofuranosyl)- and 1-(β-D-ribofuranosyl)brassenin B

Autor: Zuzana Čurillová, Peter Kutschy, Eva Solčániová, Martina Pilátová, Ján Mojžiš, and Vladimír Kováčik

Publikováno v: ARKIVOC, Vol 2008, Iss 8, Pp 85-104 (2008)

Externí odkaz: https://doaj.org/article/6813a96d72864b12958a995592a1a91c

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Synthesis of Camalexin

Autor: M. Dzurilla, M. Ruzinsky, P. Kutschy, J. Zaletova, V. Kovacik

Publikováno v: Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 6, Iss 9, Pp 716-720 (2001)
Molecules
Volume 6
Issue 9
Pages 716-720

In this paper we describe a new method for the synthesis of camalexin ( 1 )based on the reaction of 1-(tert-butoxycarbonyl)indole-3-carboxaldehyde with methyl L-cysteinate hydrochloride, followed by oxidation and decarboxylation. Compounds 1 , andint

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c33f838545a1f6d1e160424ea18ad557
http://europepmc.org/articles/PMC6236355

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Synthesis, Absolute Configuration, and Enantiomeric Enrichment of a Cruciferous Oxindole Phytoalexin, (S)-(−)-Spirobrassinin, and Its Oxazoline Analog

Autor: Milan Dzurilla, Hitoshi Goto, Mitsuo Takasugi, Nobuyuki Harada, P. Kutschy, Kenji Monde, Eva Balentova, Mojmír Suchý

Publikováno v: The Journal of Organic Chemistry. 66:3940-3947

Stereochemical studies of a cruciferous oxindole phytoalexin, (S)-(-)-spirobrassinin [(-)-4], and its oxazoline analogue, spirooxazoline (11), were carried out. Racemic spirobrassinin [(+/-)-4] was synthesized by SOCl(2)- or MsCl-mediated cyclization

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a517f5fc09b44e1916c8fbe086adbc
https://doi.org/10.1021/jo0155052

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Akademický článek

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ChemInform Abstract: Addition-Cyclization Reactions of (Z)-2,3-Diphenylpropenoyl Isothiocyanate with Aniline and Diphenylamine

Autor: Dušan Koščík, Pavol Kristian, P. Kutschy, Milan Dzurilla

Publikováno v: ChemInform. 22

tion of m-l,5,6-triphenyl-2-thiouracil. 7Vr-Phenyl-7Vr,-(2,3-diphenylpropenoyl)thiourea at similar conditions affords a mixture of cis- and trans-2-thiouracils. In the reaction with triethylamine both isomers can be iso lated. Isomerization of rrfl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::680166af2d0d38bb2af7ea98710f1d9a
https://doi.org/10.1002/chin.199131200

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