volume 7 issue 23

Studies on Synthesis of Porphyrins – β ‐Substituted with Multiple Nitrogen‐containing Groups

Publication typeJournal Article
Publication date2022-06-17
scimago Q3
wos Q3
SJR0.366
CiteScore3.0
Impact factor2.0
ISSN23656549
General Chemistry
Abstract
The preparation of highly β-substituted amino-/nitro-porphyrins is described. They were formed in two-step transformation: electrophilic nitration/nucleophilic amination via attractive substitution of hydrogen reaction (VNS). This type of porphyrins, bearing up to four nitrogen groups, are practically not available by alternative methods. They are valuable starting materials in the synthesis of more complex moieties, e. g. anticancer PDT agents.
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GOST Copy
Rosa M., Ostrowski S. Studies on Synthesis of Porphyrins – β ‐Substituted with Multiple Nitrogen‐containing Groups // ChemistrySelect. 2022. Vol. 7. No. 23.
GOST all authors (up to 50) Copy
Rosa M., Ostrowski S. Studies on Synthesis of Porphyrins – β ‐Substituted with Multiple Nitrogen‐containing Groups // ChemistrySelect. 2022. Vol. 7. No. 23.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1002/slct.202200290
UR - https://doi.org/10.1002/slct.202200290
TI - Studies on Synthesis of Porphyrins – β ‐Substituted with Multiple Nitrogen‐containing Groups
T2 - ChemistrySelect
AU - Rosa, Mariusz
AU - Ostrowski, Stanisław
PY - 2022
DA - 2022/06/17
PB - Wiley
IS - 23
VL - 7
SN - 2365-6549
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2022_Rosa,
author = {Mariusz Rosa and Stanisław Ostrowski},
title = {Studies on Synthesis of Porphyrins – β ‐Substituted with Multiple Nitrogen‐containing Groups},
journal = {ChemistrySelect},
year = {2022},
volume = {7},
publisher = {Wiley},
month = {jun},
url = {https://doi.org/10.1002/slct.202200290},
number = {23},
doi = {10.1002/slct.202200290}
}