Preparation and rearrangement study of novel thiophenium- and selenophenium-ylides

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F09%3A00021479" target="_blank" >RIV/60461373:22310/09:00021479 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Preparation and rearrangement study of novel thiophenium- and selenophenium-ylides

Original language description

A new method of synthesis of 3-substituted thieno[3,2-b][1]benzothiophenes based on a halogen dance process was developed. The cycloaddition reaction of the title compound with dimethyl acetylenedicarboxylate leads to the formation of a complex mixture of products resulting from a series of consecutive reactions of the primary adduct.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

<a href="/en/project/OC%20176" target="_blank" >OC 176: Novel monomers for liquid crystalline molecular switches</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2009

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Collection of Czechoslovak Chemical Communications

ISSN

0010-0765

e-ISSN

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Volume of the periodical

74

Issue of the periodical within the volume

5

Country of publishing house

CZ - CZECH REPUBLIC

Number of pages

14

Pages from-to

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UT code for WoS article

000267828500003

EID of the result in the Scopus database

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