An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
The1H and13C NMR and the IR spectra of the antibiotic fervenulin and its 3-substituted analogues and their 4a-indolyl derivatives are considered. Diagnostic spectral characteristics of the compounds mentioned have been revealed. Information on the structure of the 4a-indolyl derivatives of the fervenulins obtained with the aid of NMR and IR spectroscopies has been confirmed and supplemented by an x-ray structural analysis performed for crystals 4a-(indol-3-yl)-6,8-dimethyl-2,4a-5,6,7,8-hexahydropyrimido[5,4-e] [1,2,4]triazine-5,6-dione.
The1H and13C NMR and the IR spectra of the antibiotic fervenulin and its 3-substituted analogues and their 4a-indolyl derivatives are considered. Diagnostic spectral characteristics of the compounds mentioned have been revealed. Information on the structure of the 4a-indolyl derivatives of the fervenulins obtained with the aid of NMR and IR spectroscopies has been confirmed and supplemented by an x-ray structural analysis performed for crystals 4a-(indol-3-yl)-6,8-dimethyl-2,4a-5,6,7,8-hexahydropyrimido[5,4-e] [1,2,4]triazine-5,6-dione.
AbstractHeating of the diazidoalkoxytriazines (I) with aqueous acids gives the triazinetrione (II), whereas in the absence of an acid the bistetrazolylamine (III) is formed.
The paper deals with a search for new radioprotective agents containing an aminoalkane group as a pharmacophore and a pyrrolidone residue and naturally occurring fatty acid residues, which modify the hydrophobic-hydrophylic balance towards an increase in the bioavailability of an agent, as a vehicle.
AbstractBenzazolylhydrazinocarbothioamides such as (III), prepared from the hydrazinobenzazoles (I) and the isothiocyanates (II), are active against influenza A and B viruses.
ChemInformVolume 19, Issue 46 Heterocyclic Compounds ChemInform Abstract: Reaction of Fervenulin and Its 3-Substituted Analogues with Indole. YU. A. AZEV, YU. A. AZEV Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorI. I. MUDRETSOVA, I. I. MUDRETSOVA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorL. N. KURKOVSKAYA, L. N. KURKOVSKAYA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorA. F. GOLENEVA, A. F. GOLENEVA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorG. A. ALEKSANDROVA, G. A. ALEKSANDROVA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this author YU. A. AZEV, YU. A. AZEV Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorI. I. MUDRETSOVA, I. I. MUDRETSOVA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorL. N. KURKOVSKAYA, L. N. KURKOVSKAYA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorA. F. GOLENEVA, A. F. GOLENEVA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this authorG. A. ALEKSANDROVA, G. A. ALEKSANDROVA Estestv.-nauchn. inst. Permskogo univ. im. Gor'kogoSearch for more papers by this author First published: November 15, 1988 https://doi.org/10.1002/chin.198846201Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume19, Issue46November 15, 1988 RelatedInformation
AbstractReaction of antibiotic 2‐methylfervenulone (MSD‐92) (I) with nucleophiles is investigated.
ChemInformVolume 19, Issue 27 Heterocyclic Compounds ChemInform Abstract: Synthesis and Some Properties of 1,3-Dimethyl-5-nitroso-6-hydrazinouracil Derivatives. YU. A. AZEV, YU. A. AZEV Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this authorI. I. MUDRETSOVA, I. I. MUDRETSOVA Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this authorA. F. GOLENEVA, A. F. GOLENEVA Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this authorG. A. ALEXANDROVA, G. A. ALEXANDROVA Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this author YU. A. AZEV, YU. A. AZEV Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this authorI. I. MUDRETSOVA, I. I. MUDRETSOVA Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this authorA. F. GOLENEVA, A. F. GOLENEVA Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this authorG. A. ALEXANDROVA, G. A. ALEXANDROVA Ural'skii politekhn. inst. im. Kirova, SverdlovskSearch for more papers by this author First published: July 5, 1988 https://doi.org/10.1002/chin.198827183Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume19, Issue27July 5, 1988 RelatedInformation
AbstractFervenuline oxide (II) reacts with 2‐methylindole (Ib) in an acidic medium to yield the hydrazone salt (III), together with the hydrazine (IV).