Multicomponent and domino reactions of 3-aroylacrylic acids in the synthesis of heterocycles / Beryozkina Tetyana V.,Kolos Nadezhda N.,Bakulev Vasiliy A. // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2016. - V. 52, l. 9. - P. 651-657.

ISSN/EISSN:
0009-3122 / 1573-8353
Type:
Article
Abstract:
This review generalizes the data available on heterocyclizations of 3-aroylacrylic acids and their esters, published over the previous 15 years. Multicomponent, cascade, and domino reactions, as well as cycloaddition and electrocyclization reactions involving 3-aroylacrylic acids and their esters have been used to obtain five- and six-membered aromatic and non-aromatic (including chiral) oxygen- or nitrogen-containing monocyclic heterocycles, spiro compounds, as well as condensed bi- and tricyclic systems.
Author keywords:
3-aroylacrylic acids; cascade reactions; cycloaddition; domino reactions; electrocyclization; Michael addition; multicomponent reactions BETA-AROYLACRYLIC ACIDS; DIELS-ALDER REACTIONS; EFFICIENT SYNTHESIS; REGIOSELECTIVE SYNTHESIS; O-PHENYLENEDIAMINES; PUMMERER REACTION; DERIVATIVES; INHIBITORS; ALKYNES; ESTERS
DOI:
10.1007/s10593-016-1945-0
Web of Science ID:
ISI:000388588400005
Соавторы в МНС:
Другие поля
Поле Значение
Month SEP
Publisher SPRINGER
Address 233 SPRING ST, NEW YORK, NY 10013 USA
Language English
EISSN 1573-8353
Keywords-Plus BETA-AROYLACRYLIC ACIDS; DIELS-ALDER REACTIONS; EFFICIENT SYNTHESIS; REGIOSELECTIVE SYNTHESIS; O-PHENYLENEDIAMINES; PUMMERER REACTION; DERIVATIVES; INHIBITORS; ALKYNES; ESTERS
Research-Areas Chemistry
Web-of-Science-Categories Chemistry, Organic
Author-Email tetber@mail.ru
ORCID-Numbers Kolos, Nadya/0000-0002-7520-656X
Funding-Acknowledgement Russian Foundation for Basic Research {[}14-03-01033]; Ministry of Education and Science {[}4.1626.2014/K]
Funding-Text This work received financial support from the Russian Foundation for Basic Research (grant No. 14-03-01033) and the Ministry of Education and Science (State contract, project No. 4.1626.2014/K).
Number-of-Cited-References 69
Usage-Count-Last-180-days 1
Usage-Count-Since-2013 5
Journal-ISO Chem. Heterocycl. Compds.
Doc-Delivery-Number ED1EV