About: Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues Goto Sponge NotDistinct Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	skos:Concept http://linked.opendata.cz/ontology/domain/vavai/Vysledek
Description	The reaction of 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives (nitrile, amide, ethyl ester) 1 with alkylation and acylation agents were studied. Ionic 1,2-dithiole-3-ylidene amides 6 were formed in several pathways. Treatment with phosphorus pentasulfide afforded the corresponding 3,3aë4,4-trithia-1-azapentalenes 8. The results from structure study on synthesized heterocycles were described. The combination of X-ray structure analysis, IR spectroscopy, HF and DFT quantum-chemical calculation were involved. The reaction of 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives (nitrile, amide, ethyl ester) 1 with alkylation and acylation agents were studied. Ionic 1,2-dithiole-3-ylidene amides 6 were formed in several pathways. Treatment with phosphorus pentasulfide afforded the corresponding 3,3aë4,4-trithia-1-azapentalenes 8. The results from structure study on synthesized heterocycles were described. The combination of X-ray structure analysis, IR spectroscopy, HF and DFT quantum-chemical calculation were involved. (en) The reaction of 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives (nitrile, amide, ethyl ester) 1 with alkylation and acylation agents were studied. Ionic 1,2-dithiole-3-ylidene amides 6 were formed in several pathways. Treatment with phosphorus pentasulfide afforded the corresponding 3,3aë4,4-trithia-1-azapentalenes 8. The results from structure study on synthesized heterocycles were described. The combination of X-ray structure analysis, IR spectroscopy, HF and DFT quantum-chemical calculation were involved. (cs)
Title	Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues (en) Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues (cs)
skos:prefLabel	Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues (en) Syntheses and Structure Study on 3,3alambda4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues (cs)
skos:notation	RIV/00216224:14310/03:00008152!RIV08-MSM-14310___
http://linked.open.../vavai/riv/strany	1243-1263
http://linked.open...avai/riv/aktivita	P Z
http://linked.open...avai/riv/aktivity	P(GA203/01/1333), Z(MSM 143100011)
http://linked.open...iv/cisloPeriodika	7
http://linked.open...vai/riv/dodaniDat	2008
http://linked.open...aciTvurceVysledku	Pazdera, Pavel Marek, Jaromír Čmelík, Richard Čajan, Michal
http://linked.open.../riv/druhVysledku	J - Článek v odborném periodiku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Masarykova univerzita / Přírodovědecká fakulta
http://linked.open...dnocenehoVysledku	629996
http://linked.open...ai/riv/idVysledku	RIV/00216224:14310/03:00008152
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	Acylations; Alkylations; DFT calculation; Sulfur heterocycles; Trithiapenatlenes; X-Ray diffraction; Disulfides; Cyclizations (en)
http://linked.open.../riv/klicoveSlovo	DFT calculation X-Ray diffraction Acylations Alkylations Cyclizations Disulfides Sulfur heterocycles Trithiapenatlenes
http://linked.open...odStatuVydavatele	CZ - Česká republika
http://linked.open...ontrolniKodProRIV	[B34E0A7529F9]
http://linked.open...i/riv/nazevZdroje	Collection of Czechoslovak Chemical Communications
http://linked.open...in/vavai/riv/obor	CC
http://linked.open...ichTvurcuVysledku	4 (xsd:int)
http://linked.open...cetTvurcuVysledku	4 (xsd:int)
http://linked.open...vavai/riv/projekt	Chalcogen organic compounds - synthesis, transformation and structure elucidation
http://linked.open...UplatneniVysledku	2003
http://linked.open...v/svazekPeriodika	68
http://linked.open...iv/tvurceVysledku	Marek, Jaromír Pazdera, Pavel Čajan, Michal Čmelík, Richard
http://linked.open...n/vavai/riv/zamer	http://linked.opendata.cz/resource/domain/vavai/zamer/MSM%20143100011
issn	0010-0765
number of pages	11 (xsd:int)
http://localhost/t...ganizacniJednotka	14310

Faceted Search & Find service v1.16.118 as of Jun 21 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 25 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software