Synthesis of Camalexin
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 intermediates 5-7 were identified by elemental analysis...
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| Format: | Article |
| Language: | English |
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MDPI AG
2001-08-01
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| Series: | Molecules |
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| Online Access: | http://www.mdpi.com/1420-3049/6/9/716/ |
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doaj-ee6f361518d64b809f201d31a046525b2020-11-25T01:47:46ZengMDPI AGMolecules1420-30492001-08-016971672010.3390/60900716Synthesis of CamalexinV. KovacikM. RuzinskyJ. ZaletovaP. KutschyM. DzurillaIn 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 intermediates 5-7 were identified by elemental analysis, 1H NMR, 13C NMR and mass spectroscopy.http://www.mdpi.com/1420-3049/6/9/716/Camalexinphytoalexinsindoles |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
V. Kovacik M. Ruzinsky J. Zaletova P. Kutschy M. Dzurilla |
| spellingShingle |
V. Kovacik M. Ruzinsky J. Zaletova P. Kutschy M. Dzurilla Synthesis of Camalexin Molecules Camalexin phytoalexins indoles |
| author_facet |
V. Kovacik M. Ruzinsky J. Zaletova P. Kutschy M. Dzurilla |
| author_sort |
V. Kovacik |
| title |
Synthesis of Camalexin |
| title_short |
Synthesis of Camalexin |
| title_full |
Synthesis of Camalexin |
| title_fullStr |
Synthesis of Camalexin |
| title_full_unstemmed |
Synthesis of Camalexin |
| title_sort |
synthesis of camalexin |
| publisher |
MDPI AG |
| series |
Molecules |
| issn |
1420-3049 |
| publishDate |
2001-08-01 |
| description |
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 intermediates 5-7 were identified by elemental analysis, 1H NMR, 13C NMR and mass spectroscopy. |
| topic |
Camalexin phytoalexins indoles |
| url |
http://www.mdpi.com/1420-3049/6/9/716/ |
| work_keys_str_mv |
AT vkovacik synthesisofcamalexin AT mruzinsky synthesisofcamalexin AT jzaletova synthesisofcamalexin AT pkutschy synthesisofcamalexin AT mdzurilla synthesisofcamalexin |
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