3-Carboxylate-Substituted Isoindolinones in K2CO3-Catalyzed Michael Reactions
Publication type: Journal Article
Publication date: 2015-04-29
scimago Q3
wos Q3
SJR: 0.322
CiteScore: 4.3
Impact factor: 1.8
ISSN: 00397911, 15322432
Organic Chemistry
Abstract
AbstractActivated 3-substituted isoindolinones have proved to be efficient nucleophiles in K2CO3-catalyzed Michael reactions of several types of electron-deficient olefins. Moreover, tricyclic pyrrolizidines have been conveniently synthesized via a modification of the described general protocol as a consequence of a cascade Michael/cyclization reaction of unsaturated aldehydes.
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Total citations:
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Scorzelli F. et al. 3-Carboxylate-Substituted Isoindolinones in K2CO3-Catalyzed Michael Reactions // Synthetic Communications. 2015. Vol. 45. No. 13. pp. 1552-1558.
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Scorzelli F., Di Mola A., Palombi L., Filosa R., Massa A. 3-Carboxylate-Substituted Isoindolinones in K2CO3-Catalyzed Michael Reactions // Synthetic Communications. 2015. Vol. 45. No. 13. pp. 1552-1558.
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TY - JOUR
DO - 10.1080/00397911.2015.1033063
UR - https://doi.org/10.1080/00397911.2015.1033063
TI - 3-Carboxylate-Substituted Isoindolinones in K2CO3-Catalyzed Michael Reactions
T2 - Synthetic Communications
AU - Scorzelli, Francesco
AU - Di Mola, Antonia
AU - Palombi, Laura
AU - Filosa, Rosanna
AU - Massa, Antonio
PY - 2015
DA - 2015/04/29
PB - Taylor & Francis
SP - 1552-1558
IS - 13
VL - 45
SN - 0039-7911
SN - 1532-2432
ER -
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BibTex (up to 50 authors)
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@article{2015_Scorzelli,
author = {Francesco Scorzelli and Antonia Di Mola and Laura Palombi and Rosanna Filosa and Antonio Massa},
title = {3-Carboxylate-Substituted Isoindolinones in K2CO3-Catalyzed Michael Reactions},
journal = {Synthetic Communications},
year = {2015},
volume = {45},
publisher = {Taylor & Francis},
month = {apr},
url = {https://doi.org/10.1080/00397911.2015.1033063},
number = {13},
pages = {1552--1558},
doi = {10.1080/00397911.2015.1033063}
}
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MLA
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Scorzelli, Francesco, et al. “3-Carboxylate-Substituted Isoindolinones in K2CO3-Catalyzed Michael Reactions.” Synthetic Communications, vol. 45, no. 13, Apr. 2015, pp. 1552-1558. https://doi.org/10.1080/00397911.2015.1033063.