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AbstractAbstract
No abstract available
Original Title
Ehkstraktsionno-fotometricheskoe opredelenie indiya i galliya s pomoshch'yu 5,7-dibrom-oksikhinolina
Primary Subject
Record Type
Journal Article
Literature Type
Progress Report
Journal
Ukrainskij Khimicheskij Zhurnal; v. 36(12); p. 1273-1278
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INIS VolumeINIS Volume
INIS IssueINIS Issue
Blackburn, C.E.
Centre d'Etude de l'Energie Nucleaire, Mol (Belgium)1970
Centre d'Etude de l'Energie Nucleaire, Mol (Belgium)1970
AbstractAbstract
No abstract available
Primary Subject
Record Type
Journal Article
Literature Type
Progress Report
Journal
Journal of Labelled Compounds; v. 6(1); p. 21-33
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INIS VolumeINIS Volume
INIS IssueINIS Issue
AbstractAbstract
No abstract available
Original Title
Ehkstraktsiya toriya iz azotnokislykh sred 1, 3, 4, 5- tetrazameshchennymi pirazolami
Primary Subject
Record Type
Journal Article
Literature Type
Progress Report
Journal
Zhurnal Neorganicheskoj Khimii; v. 16(5); p. 1401-1406
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INIS VolumeINIS Volume
INIS IssueINIS Issue
AbstractAbstract
No abstract available
Original Title
Polimerizatsiya i sopolimerizatsiya N-arilmal'imidov pod dejstviem γ-izlucheniya Co60
Record Type
Journal Article
Journal
Vysokomol. Soedin; v. 13(5); p. 334-337
Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
Masse, Bernard.
CEA Centre d'Etudes Nucleaires de Saclay, 91 - Gif-sur-Yvette (France). Dept. des Radioelements; Lyon Univ., 69 (France). Faculte des Sciences1971
CEA Centre d'Etudes Nucleaires de Saclay, 91 - Gif-sur-Yvette (France). Dept. des Radioelements; Lyon Univ., 69 (France). Faculte des Sciences1971
AbstractAbstract
No abstract available
Original Title
Syntheses de pyrimidines, de purines et des nucleosides correspondants marques par le carbone 14 a partir de derives trimethylsilyles
Primary Subject
Source
Jan 1971; 170 p; These (D. es S.).
Record Type
Report
Literature Type
Thesis/Dissertation
Report Number
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Reference NumberReference Number
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INIS IssueINIS Issue
AbstractAbstract
No abstract available
Primary Subject
Record Type
Journal Article
Journal
J. Chem. Soc., D; (no.20); p. 1304-1305
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Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
Kutacek, M.; Kralova, M.; Hofinger, M.
6. radiochemical conference on preparative methods, analytical procedures, stability of labelled compounds1971
6. radiochemical conference on preparative methods, analytical procedures, stability of labelled compounds1971
AbstractAbstract
No abstract available
Primary Subject
Source
Ceskoslovenska Akademie Ved, Prague. Ceskoslovenska Spolecnost Chemicka; Ceskoslovenska Komise pro Atomovou Energii, Prague; Ustav pro Vyzkum, Vyrobu a Vyuziti Radioisotopu, Prague (Czechoslovakia); Ceskoslovenska Akademie Ved, Rez. Ustav Jaderneho Vyzkumu; Ceskoslovenska Akademie Ved, Prague. Isotopova Laborator Biologickych Ustavu; p. 15-16; 1971; 6. radiochemical conference on the methods of preparation, storage and control of labelled compounds; Marianske Lazne, Czechoslovakia; 3 May 1971
Record Type
Report
Literature Type
Conference
Report Number
Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
AbstractAbstract
[en] Alkylarylketiminoboranes react with nitriles to from boron β-diiminates whose structure is established on the basis of ultraviolet, infrared, PMR, and 11B NMR spectra. Depending on their structure, β-diiminates are hydrolysed in acid medium to form either boron β-diketonates, or β-diketones. Upon interaction of boron β-diiminates with HCl or HBF4 boronium salts are formed with β-diimines as ligands
Original Title
Bororganicheskie soedineniya
Primary Subject
Source
12 refs.; for English translation see the journal Bull. Acad. Sci. USSR, Div. Chem. Sci.
Record Type
Journal Article
Journal
Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (no.12); p. 2756-2762
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Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
AbstractAbstract
No abstract available
Original Title
Prisoedinenie enaminodialkilboranov k izonitrilam
Primary Subject
Source
Published in summary form only; for English translation see the journal Bull. Acad. Sci. USSR, Div. Chem. Sci.
Record Type
Journal Article
Journal
Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (no.6); p. 1431
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AbstractAbstract
[en] α-Sulfenylation of aldehydes and ketones using N-formyl and N-acyl sulfenamides, prepared by Cu-catalyzed aerobic coupling of amides and thiols, was achieved in the presence of cyclic secondary amine⋅HCl catalysts. To obtain various sulfur-functionalized carbonyl compounds, sulfenamides containing aromatic and aliphatic organosulfur were investigated. As carbonyl compounds, cyclic and acyclic ketones, 1,3-dicarbonyl compounds, and aldehydes were investigated, affording the desired α-sulfenylation products in good yields
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Secondary Subject
Source
17 refs, 6 figs, 9 tabs
Record Type
Journal Article
Journal
Bulletin of the Korean Chemical Society; ISSN 0253-2964;
; v. 38(3); p. 389-391

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