volume 62 issue 31 pages 7213-7256

Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions

Publication typeJournal Article
Publication date2006-07-01
scimago Q3
wos Q2
SJR0.426
CiteScore4.1
Impact factor2.2
ISSN00404020, 14645416
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
The methods used for the synthesis of vicinal diaryl-substituted pyrrole, pyrroline and pyrrolidine derivatives are reviewed. The report which contains 461 references also summarizes the bioactivity data of some of these compounds. Figure options Download full-size image Download as PowerPoint slide
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GOST |
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GOST Copy
Bellina F., Rossi R. Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions // Tetrahedron. 2006. Vol. 62. No. 31. pp. 7213-7256.
GOST all authors (up to 50) Copy
Bellina F., Rossi R. Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions // Tetrahedron. 2006. Vol. 62. No. 31. pp. 7213-7256.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.tet.2006.05.024
UR - https://doi.org/10.1016/j.tet.2006.05.024
TI - Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions
T2 - Tetrahedron
AU - Bellina, Fabio
AU - Rossi, Renzo
PY - 2006
DA - 2006/07/01
PB - Elsevier
SP - 7213-7256
IS - 31
VL - 62
SN - 0040-4020
SN - 1464-5416
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2006_Bellina,
author = {Fabio Bellina and Renzo Rossi},
title = {Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions},
journal = {Tetrahedron},
year = {2006},
volume = {62},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/j.tet.2006.05.024},
number = {31},
pages = {7213--7256},
doi = {10.1016/j.tet.2006.05.024}
}
MLA
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MLA Copy
Bellina, Fabio, and Renzo Rossi. “Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions.” Tetrahedron, vol. 62, no. 31, Jul. 2006, pp. 7213-7256. https://doi.org/10.1016/j.tet.2006.05.024.